Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448211생성일: 2026년 10월 25일
Cesium carbonate → Methyl 2-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)-5-oxohexanoate
https://huagongshe.com/reaction/448211
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 1-(3-Chlorophenyl)propan-2-one | HCID 2734097 | — |
| 반응물 | (S)-Methyl 2-Boc-amino-3-iodopropionate | HCID 11416215 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl 2-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)-5-oxohexanoate | HCID 68750611 | — |
반응 단계
A mixture of cesium carbonate (9.80 g, 30.1 mmol) and methyl N-(tert-butoxycarbonyl)-3-iodo-D-alaninate (9.90 g, 30.1 mmol) in DMF (75 mL) was stirred at 23° C. for 45 min before 1-(3-chlorophenyl)propan-2-one (6.09 g, 36.1 mmol) and additional cesium carbonate (9.80 g, 30.1 mmol) were added. The resulting mixture was stirred for 2.5 h. The majority of the DMF was then removed under reduced pressure at a bath temperature of <40° C. The concentrated mixture was partitioned between water (500 mL) and ethyl acetate (2×200 mL). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to give the title compound as a 1:1 racemic mixture of diastereomers, which was used without further purification. MS: m/z=314.1 (M-t-Bu+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08481556B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-fb9c714847054ac89c96f851bf265097 |
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| 출처 메모 | uspto-grants-2013_07 |
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