참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | DL-Homoserine | HCID 779 | — |
| 반응물 | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (RS)-2-(4-chlorobenzenesulfonylamino)-4-butanolide | HCID 19032731 | 60.6% |
반응 단계
(RS)-2-amino-4-hydroxybutanoic acid (2.0438 g) was dissolved in water (20 ml). The solution was cooled to 0° C., and potassium carbonate (5.217 g) and ethyl acetate (20 ml) were added. Then, p-chlorobenzenesulfonyl chloride (9.0536 g) and THF (2 ml) were added, and the whole was stirred overnight. After the reaction was completed, the ethyl acetate layer was separated. The aqueous layer was acidified with 2N HCl and extracted with ethyl acetate. The combined ethyl acetate layers were concentrated to give a crude product. The crude product was purified by silica gel column chromatography (silica gel 50 g, hexane/ethyl acetate=2/1) to obtain (RS)-2-(4-chlorobenzenesulfonylamino)-4-butanolide (2.8674 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05650428 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-b9c6c5a45e164ac8aa66d3c6f2f83ebc |
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| 출처 메모 | uspto-grants-1997_07 |
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