참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexamethylphosphoramide | HCID 12679 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Ethyl 5-(2-formyl-3-hydroxyphenoxy)pentanoate | HCID 9838209 | — |
| 반응물 | Sodium thiocresolate | HCID 86739085 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 5-(2-Formyl-3-hydroxyphenoxy)pentanoic acid | HCID 72162 | — |
반응 단계
Ethyl 5-(2-formyl-3-methoxphenoxy)pentanoate (Example 4) (2.0 g, 0.00704 M), sodium thiocresolate (2.06 g, 0.014 M), hexamethylphosphoramide (2.48 ml, 0.014 M) and benzene (10 ml) were placed in a round bottom flask and refluxed for 18 hours. The reaction mixture, containing ethyl 5-(2-formyl-3-hydroxyphenoxy)pentanoate, was then cooled and poured into 2 N sodium hydroxide solution (20 ml). The organic layer was removed, diluted with ether (20 ml), then extracted with 2 N sodium hydroxide solution (2×20 ml). The aqueous layers were combined and extracted with dichloromethane (2×20 ml). The organic layer was discarded and the aqueous layer acidified with concentrated hydrochloric acid. The resulting precipitate was filtered, washed with water and dried in a desiccator over phosphorus pentoxide to give 5-(2-formyl-3-hydroxyphenoxy)pentanoic acid, m.p. 98°-99° C. from ethyl acetate/petrol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04410537 |
|---|
| 출처 데이터셋 | uspto-grants-1983_10 |
|---|
| ORD ID | ord-261005c37ffd402fb2238eacd4b34f05 |
|---|
| 출처 메모 | uspto-grants-1983_10 |
|---|