BE605331A - - Google Patents
Info
- Publication number
- BE605331A BE605331A BE605331DA BE605331A BE 605331 A BE605331 A BE 605331A BE 605331D A BE605331D A BE 605331DA BE 605331 A BE605331 A BE 605331A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- distillation
- triethylborine
- recovered
- reacted
- Prior art date
Links
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical compound CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- -1 halide radicals Chemical class 0.000 claims description 10
- 238000004821 distillation Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 229910052796 boron Inorganic materials 0.000 claims description 6
- 125000005234 alkyl aluminium group Chemical group 0.000 claims description 4
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 3
- CQYBWJYIKCZXCN-UHFFFAOYSA-N diethylaluminum Chemical compound CC[Al]CC CQYBWJYIKCZXCN-UHFFFAOYSA-N 0.000 claims description 2
- 150000001639 boron compounds Chemical class 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- 229910015900 BF3 Inorganic materials 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000001642 boronic acid derivatives Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- YLYNVLJAZMTTIQ-UHFFFAOYSA-N butoxy(diethyl)alumane Chemical compound CCCC[O-].CC[Al+]CC YLYNVLJAZMTTIQ-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
- 210000000941 bile Anatomy 0.000 description 1
- 101150037462 ccmE gene Proteins 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000003822 preparative gas chromatography Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- LHJSLDBKUGXPMI-UHFFFAOYSA-N tris(2-methylpropyl) borate Chemical compound CC(C)COB(OCC(C)C)OCC(C)C LHJSLDBKUGXPMI-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/027—Organoboranes and organoborohydrides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE605331A true BE605331A (2) |
Family
ID=192815
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE605331D BE605331A (2) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE605331A (2) |
-
0
- BE BE605331D patent/BE605331A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO171676B (no) | Dietere anvendelige ved fremstilling av ziegler-natta-katalysatorer | |
| US4599440A (en) | Organocyclosiloxane | |
| EP3347339B1 (fr) | Composés étheramines et leur utilisation en tant que collecteur de flottation | |
| JPS6296451A (ja) | フロオロアルキル（メタ）アクリレ−トの製造法 | |
| BE605331A (2) | ||
| EP0300862A2 (fr) | Composition à base d'un nouveau polycarbosilane, sa préparation et son application à la fabrication de produits et articles céramiques à base de carbure de silicium | |
| NO126273B (2) | ||
| CN1539841A (zh) | 新型铋化合物、其制备方法和膜的制备方法 | |
| JP6908453B2 (ja) | オルガノキシシロキサンの製造法及びホウ素化合物 | |
| JP5374774B2 (ja) | 金属シクロペンタジエンナイドの製造方法 | |
| US6476279B2 (en) | Method of making fluorinated alcohols | |
| CN114057782B (zh) | 一种合成4-巯基苯硼酸的工艺方法 | |
| CN115368235B (zh) | 一种三氟乙酸乙酯的制备方法 | |
| US4996340A (en) | Intramolecular migration reactions | |
| BE592657A (2) | ||
| RU2833785C1 (ru) | Способ получения 1-(3-(триметоксисилил)пропил)бензимидазола | |
| US3070631A (en) | Process for the preparation of alkylborines | |
| RU2716710C1 (ru) | Новые мононатриевые соли органоалкоксисиланов и способ их получения | |
| US2090485A (en) | Dialkylaminoalcohols | |
| KR102460443B1 (ko) | 지환성 아크릴유도체의 제조 방법 | |
| JP2967171B1 (ja) | ペルフルオロアルキル基含有ヨウ化アルキルの製造方法 | |
| SU325847A1 (ru) | Способ получения галлийтриалкилов | |
| CA1134379A (en) | Process for synthesising alkoxyalanates of alkaline earth metals | |
| JPS5829731A (ja) | 酸化防止剤の製造方法 | |
| US4005104A (en) | Products from the reaction of sulfur trioxide with acyclic internal vic-dialkoxypolyfluoroalkenes |