Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 714127생성일: 2026년 10월 25일
Potassium Carbonate → tert-butyl[(2S,3E)-1-{[tert-butyl(diphenyl)silyl]oxy}-4-(2-nitrophenyl)but-3-en-2-yl]carbamate
https://huagongshe.com/reaction/714127
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | Phosphonium | HCID 5460504 | — |
| 반응물 | (2-Nitrobenzyl)triphenylphosphonium bromide | HCID 10885283 | — |
| 반응물 | tert-butyl[(2R)-1-{[tert-butyl(diphenyl)silyl]oxy}-3-oxopropan-2-yl]carbamate | HCID 89929680 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | tert-butyl[(2S,3E)-1-{[tert-butyl(diphenyl)silyl]oxy}-4-(2-nitrophenyl)but-3-en-2-yl]carbamate | HCID 131734057 | 38.1% |
반응 단계
A solution of tert-butyl[(2R)-1-{[tert-butyl(diphenyl)silyl]oxy}-3-oxopropan-2-yl]carbamate (3, 3.12 g, 7.3 mmol) in DME (30 ml) was treated with solid (2-nitrobenzyl)(triphenyl)phosphonium bromide(3.76 g, 7.86 mmol) (or any other suitable phosphonium salt), the mixture stirred at room temperature under N2 atmosphere for 30 min and then the reaction flask was charged with a solid mixture of potassium carbonate (1.78 g, 12.86 mmol) and 18-crown-6 (219 mg, 0.83 mmol). The purple mixture was further stirred at the same temperature for 14 h; diluted with DCM, washed with saturated NaHCO3, dried over MgSO4, filtered and concentrated Purified through a chromatographic cartridge of silicagel (50 g) eluted with 10% to 35% EtOAc in hexane to get 1.52 g (38% yield) of title compound as light yellow oil. MS: m/z=569.2 (MNa+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09187415B2 |
|---|
| 출처 데이터셋 | uspto-grants-2015_11 |
|---|
| ORD ID | ord-13cfa7bc3a9f4e0a87920188b63cd6d6 |
|---|
| 출처 메모 | uspto-grants-2015_11 |
|---|