Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16323생성일: 2026년 10월 26일
Tetrahydrofuran → tert-butyl [(1R,2S)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]carbamate
https://huagongshe.com/reaction/16323
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Carbonic acid, bis(1,1-dimethylethyl) ester | HCID 10219638 | — |
| 반응물 | (1R,2S)-1-azido-1-(3,4,5-trifluorophenyl)propan-2-ol | HCID 86612610 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | tert-butyl [(1R,2S)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]carbamate | HCID 68717988 | 86.3% |
반응 단계
In nitrogen atmosphere, triphenylphosphine (5.85 g) was added to a THF solution (75 mL) of (1R,2S)-1-azido-1-(3,4,5-trifluorophenyl)propan-2-ol (5.16 g). This reaction solution was stirred at room temperature for 10 min, then water (5 mL) was added the reaction solution. This mixture was stirred at 60° C. for 3.5 hr. The reaction solution was cooled to room temperature, and then di-tert-butylcarbonate (5.35 g) was added to the reaction solution. The resulting reaction solution was stirred at room temperature for 45 min and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (toluene:ethyl acetate=9:1) to give 5.88 g of the title compound. The physical property values of this compound 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-9b929db65e1f4d39ba38def4d69f12d7 |
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| 출처 메모 | uspto-grants-2010_06 |
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