Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16375생성일: 2026년 10월 23일
{(1R,2R)-2-benzyloxy-1-[(methoxymethylcarbamoyl)methoxymethyl]propyl}carbamic acid t-butyl ester → {(1R,2R)-2-benzyloxy-1-[2-(4-chlorophenyl)-2-oxoethoxymethyl]propyl}carbamic acid t-butyl ester
https://huagongshe.com/ko/reaction/16375
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | {(1R,2R)-2-benzyloxy-1-[(methoxymethylcarbamoyl)methoxymethyl]propyl}carbamic acid t-butyl ester | HCID 67379173 | — |
| 반응물 | HCID 178478191 | HCID 178478191 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | {(1R,2R)-2-benzyloxy-1-[2-(4-chlorophenyl)-2-oxoethoxymethyl]propyl}carbamic acid t-butyl ester | HCID 67373088 | — |
반응 단계
A solution of {(1R,2R)-2-benzyloxy-1-[(methoxymethylcarbamoyl)methoxymethyl]propyl}carbamic acid t-butyl ester (2.42 g) in tetrahydrofuran (50 mL) was cooled to −40° C. and to the mixture was then dropwise added 4-chlorophenylmagnesium bromide (18.3 mL, 1 M tetrahydrofuran solution). The resultant solution was stirred for 1 hour at −40° C., after which the temperature was slowly raised to 0° C. The solution was then diluted with saturated aqueous ammonium chloride. The resultant solution was extracted using ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate. Solvent was removed by distillation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (heptane/ethyl acetate 9/1→1/1), to thereby obtain the titled compound (2.61 g). The physical properties of this crude product were as follows.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737141B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-4c957e16d1a84e578fc1b0ae8c2d812d |
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| 출처 메모 | uspto-grants-2010_06 |
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