JPS6132A - アルコ−ル分離剤 - Google Patents

アルコ−ル分離剤

Info

Publication number: JPS6132A
Authority: JP; Japan
Prior art keywords: alcohol; compound; formula; separating agent; lower alkyl
Prior art date: 1984-06-09
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

JP11859384A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0414653B2 (de

Inventor

Fumio Toda

芙三夫戸田

Koichi Tanaka

耕一田中

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Individual

Original Assignee

Individual

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-06-09

Filing date

1984-06-09

Publication date

1986-01-06

1984-06-09 Application filed by Individual filed Critical Individual

1984-06-09 Priority to JP11859384A priority Critical patent/JPS6132A/ja

1986-01-06 Publication of JPS6132A publication Critical patent/JPS6132A/ja

1992-03-13 Publication of JPH0414653B2 publication Critical patent/JPH0414653B2/ja

Status Granted legal-status Critical Current

Links

LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 55
125000000217 alkyl group Chemical group 0.000 claims abstract description 14
239000003795 chemical substances by application Substances 0.000 claims abstract description 12
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract description 8
-1 acetylene alcohol compound Chemical class 0.000 claims description 11
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 6
150000001875 compounds Chemical class 0.000 abstract description 26
239000013078 crystal Substances 0.000 abstract description 10
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 6
150000001298 alcohols Chemical class 0.000 abstract description 4
238000006243 chemical reaction Methods 0.000 abstract description 4
238000001035 drying Methods 0.000 abstract description 3
238000001914 filtration Methods 0.000 abstract description 3
239000002244 precipitate Substances 0.000 abstract description 3
238000000926 separation method Methods 0.000 abstract description 3
ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 abstract description 3
238000011084 recovery Methods 0.000 abstract 2
150000008366 benzophenones Chemical class 0.000 abstract 1
125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
235000019441 ethanol Nutrition 0.000 description 47
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 5
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
238000011160 research Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
WCASXYBKJHWFMY-NSCUHMNNSA-N 2-Buten-1-ol Chemical compound C\C=C\CO WCASXYBKJHWFMY-NSCUHMNNSA-N 0.000 description 1
UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 1
AHEOVUWANYQNIZ-UHFFFAOYSA-N 9-prop-1-ynylfluoren-9-ol Chemical compound C1=CC=C2C(C#CC)(O)C3=CC=CC=C3C2=C1 AHEOVUWANYQNIZ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
235000010633 broth Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000012230 colorless oil Substances 0.000 description 1
230000009918 complex formation Effects 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
WCASXYBKJHWFMY-UHFFFAOYSA-N gamma-methylallyl alcohol Natural products CC=CCO WCASXYBKJHWFMY-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000011707 mineral Substances 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
238000012827 research and development Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP11859384A 1984-06-09 1984-06-09 アルコ−ル分離剤 Granted JPS6132A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP11859384A JPS6132A (ja)	1984-06-09	1984-06-09	アルコ−ル分離剤

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP11859384A JPS6132A (ja)	1984-06-09	1984-06-09	アルコ−ル分離剤

Publications (2)

Publication Number	Publication Date
JPS6132A true JPS6132A (ja)	1986-01-06
JPH0414653B2 JPH0414653B2 (de)	1992-03-13

Family

ID=14740419

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11859384A Granted JPS6132A (ja)	1984-06-09	1984-06-09	アルコ−ル分離剤

Country Status (1)

Country	Link
JP (1)	JPS6132A (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4500907A (en) *	1981-10-23	1985-02-19	Tokyo Shibaura Denki Kabushiki Kaisha	Pressure-applied type semiconductor device

1984
- 1984-06-09 JP JP11859384A patent/JPS6132A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4500907A (en) *	1981-10-23	1985-02-19	Tokyo Shibaura Denki Kabushiki Kaisha	Pressure-applied type semiconductor device

Also Published As

Publication number	Publication date
JPH0414653B2 (de)	1992-03-13

Publication	Publication Date	Title
TW458961B (en)	2001-10-11	Amino acid-derived diaminopropanols
Hinman et al.	1959	Alkylation of Acylhydrazines. The Synthesis of Trimethylamine-benzimide
US3105854A (en)	1963-10-01	Meta-substituted phenoxyethylamines
JPS6132A (ja)	1986-01-06	アルコ−ル分離剤
JPH06500094A (ja)	1994-01-06	プロピルアミン誘導体
Blackwood et al.	1958	The Synthesis of 6-Chloropyridoxine. The Hydride Reduction of Pyridinedicarboxylic Acids
CN115745847A (zh)	2023-03-07	一种n-n类化合物及其偶联制备方法
JPS60104060A (ja)	1985-06-08	置換アゼチジン誘導体、それらの製造方法およびそれらの中間体としての使用
US3317560A (en)	1967-05-02	Indol-3-yl alkylguanidine derivatives
JPH04149151A (ja)	1992-05-22	４―ブロモ―３―ヒドロキシ酪酸エステル誘導体の製造法
JPH033675B2 (de)	1991-01-21
US3467710A (en)	1969-09-16	Beta-(4- or 5-phenyl-1-naphthalene) ethylamines
US3366686A (en)	1968-01-30	Process for preparing primary amines
US2418237A (en)	1947-04-01	Process for preparation of 2, 2-dialkyl-1, 3-propanediamines
JP3175253B2 (ja)	2001-06-11	単環式含窒素複素環化合物をゲストとする新規包接化合物
Barassi et al.	1994	Organomercury Compounds. 32. Syntheses of Fluorophenylmercurials by Decarboxylation
US4769502A (en)	1988-09-06	Alkynol type compounds and alcohol-separating process
JPS6365053B2 (de)	1988-12-14
JPS62145082A (ja)	1987-06-29	（＋／−）１４，１５−ジヒドロ−（３β，１４α，１６α）−２０，２１−ジノルエブルナメニン−１４−オ−ルの調製方法
IL25717A (en)	1970-01-29	9-((2-amino-1-methyl)ethyl)fluoren-9-ols and process for the preparation thereof
CA1065868A (en)	1979-11-06	Mono fumarate of 3-pyridymethyl nicotinate and a process for the preparation thereof
CA1187490A (en)	1985-05-21	Process for the production of ketoamines
US3080373A (en)	1963-03-05	Diallyl-nortoxiferine dihalides
JPH0419975B2 (de)	1992-03-31
US3776946A (en)	1973-12-04	Chlorphenesin derivatives

JPS6132A - アルコ−ル分離剤 - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=14740419

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

Also Published As

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