CH100355A - Process for the preparation of an aryloxynaphthyl ketone. - Google Patents
Process for the preparation of an aryloxynaphthyl ketone.Info
- Publication number
- CH100355A CH100355A CH100355DA CH100355A CH 100355 A CH100355 A CH 100355A CH 100355D A CH100355D A CH 100355DA CH 100355 A CH100355 A CH 100355A
- Authority
- CH
- Switzerland
- Prior art keywords
- ketone
- benzotrichloride
- act
- allowed
- aryloxynaphthyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 150000002576 ketones Chemical class 0.000 title description 2
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 3
- 239000003518 caustics Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 230000007717 exclusion Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims 2
- 239000003513 alkali Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
- C07C49/83—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups polycyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/008—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with tri- or tetrahalomethyl compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
verfahren zur Herstellung eines Aryloxynaphtylketons. Es wurde gefunden, dass man ein Aryloxy- na.plity llzeton herstellen kann, wenn man auf ss-Naplithol, mit oder ohne Zusatz von Ver- dünnunl;s- bezw. Kondensationsmitteln, aber unter Ausschluss von Alkalien, Belizotriehlo- rid einwirken lässt.
Das so gewonnene 1 . 1'- PhenyInaplity 1 - 2'- oxy - keton bildet weisse Nadeln, !die bei 175 schmelzen und sich in Ätzalkalien und in konzentrierter Schwefel säure mit gelber Farbe lösen. Beispiel: 19,,i. Teile Benzotrichlorid und 14,4 Teile ss-Nalilitliol werden unter Kühlung in 100 Teile konzentrierte Schwefelsäure eingetra gen und so lange zusammen gerührt, bis sich keine Salzsäure mehr entwickelt.
Hierauf giesst man in Wasser, filtriert das ausge schiedene 1 . l.'-Plienylnaphtyl - 2'-oxy-keton ab und .reinigt es durch Umkristallisieren seines Natriumsalzes.
process for the production of an aryloxynaphthyl ketone. It has been found that an aryloxyna.plity llteton can be produced by using ss-naplithol, with or without the addition of thinner or thinner. Condensation agents, but with the exclusion of alkalis, allows belizotri chloride to act.
The 1. 1'- PhenyInaplity 1 - 2'- oxy - ketone forms white needles! Which melt at 175 and dissolve in caustic alkalis and in concentrated sulfuric acid with a yellow color. Example: 19,, i. Parts of benzotrichloride and 14.4 parts of ß-nalilitliol are introduced into 100 parts of concentrated sulfuric acid with cooling and stirred together until hydrochloric acid no longer develops.
It is then poured into water, the precipitated 1 is filtered off. l'-Plienylnaphtyl - 2'-oxy-ketone and purifies it by recrystallizing its sodium salt.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH100355T | 1921-09-24 | ||
| CH98559T | 1921-09-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH100355A true CH100355A (en) | 1923-07-16 |
Family
ID=25705426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH100355D CH100355A (en) | 1921-09-24 | 1921-09-24 | Process for the preparation of an aryloxynaphthyl ketone. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH100355A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3526666A (en) * | 1968-01-12 | 1970-09-01 | Ferro Corp | Synthesis of 2-hydroxy-4-alkoxybenzophenones |
-
1921
- 1921-09-24 CH CH100355D patent/CH100355A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3526666A (en) * | 1968-01-12 | 1970-09-01 | Ferro Corp | Synthesis of 2-hydroxy-4-alkoxybenzophenones |
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