Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 987920생성일: 2026년 10월 25일
Cerium(III) chloride → 4-Benzyl-5-(2-tert-butylcarbamoyl-4-hydroxy-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/987920
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cerium(III) chloride | HCID 24636 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 4-Benzyl-5-(2-tert-butylcarbamoyl-4-oxo-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester | HCID 69854080 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 4-Benzyl-5-(2-tert-butylcarbamoyl-4-hydroxy-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester | HCID 69854782 | 77.8% |
반응 단계
A solution of 4-benzyl-5-(2-tert-butylcarbamoyl-4-oxo-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (1.1 g, 2.2 mmol) in dry methanol (20 ml) was stirred at room temperature under nitrogen during the addition of cerium chloride (1.8 g, 4.84 mmol). The resulting mixture was stirred at room temperature for 30 minutes, then cooled to −78° C. and treated with sodium borohydride (183 mg, 4.84 mmol). The resulting suspension was allowed to warm to 0° C. over 90 min, then partitioned between ethyl acetate and a mixture of saturated aqueous ammonium chloride solution and brine. The two layers were separated and the aqueous phase was extracted twice with ethyl acetate. The combined organic layers were dried (anhydrous magnesium sulfate) and concentrated in vacuo. Purification by flash chromatography on silica gel (ethyl acetate/hexane: 1/1 to 2/1) provided 4-benzyl-5-(2-tert-butylcarbamoyl-4-hydroxy-cyclohexylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (860 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06632826B1 |
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| 출처 데이터셋 | uspto-grants-2003_10 |
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| ORD ID | ord-8d2d03d10be3438e94fcce368d028557 |
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| 출처 메모 | uspto-grants-2003_10 |
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