Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → (4R)-3-[3-(2-Carboxyethyldisulfanyl)propanoyl]-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (4R)-2-(2-hydroxyphenyl)-1,3-thiazolidine-4-carboxylic acid | HCID 2825745 | — |
| 반응물 | 1,5,6-Oxadithionane-2,9-dione | HCID 54294599 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | (4R)-3-[3-(2-Carboxyethyldisulfanyl)propanoyl]-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid | HCID 13053751 | — |
반응 단계
To a stirred solution of 2.0 g of (4R)-2-hydroxyphenyl-4-thiazolidinecarboxylic acid and 1.7 ml of triethylamine in 15 ml of anhydrous acetone, 2.0 g of dithiodipropanoic anhydride is added. The resulting mixture is continuously stirred for 40 min at room temperature and extracted with ethyl acetate after addition of 50 ml of water containing a small amount of potassium carbonate. The aqueous layer is acidified with N aqueous hydrochloric acid and extracted with ethyl acetate. The second organic layer is washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residual oil is purified by column chromatography on silica gel to give crystals of the titled compound. The yield is 0.6 g (15%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04410542 |
| 출처 데이터셋 | uspto-grants-1983_10 |
| ORD ID | ord-0be0cd70bff4422d92c316d2e1d9d1de |
| 출처 메모 | uspto-grants-1983_10 |