Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl iodide → tert-butyl N-benzyloxy-N-methylcarbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Tert-butyl N-(benzyloxy)carbamate | HCID 736159 | — |
| 반응물 | tert-butyl N-benzyloxy-N-(2-methylpropyl)carbamate | HCID 19967428 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | tert-butyl N-benzyloxy-N-methylcarbamate | HCID 14227181 | — |
반응 단계
Sodium hydride (0.48 g of 80% in mineral oil, 16 mmol) was added to a solution of tert-butyl N-benzyloxycarbamate (Compound 54 Part A, 3 g, 13 mmol) in N,N-dimethylformamide (25 mL). The reaction mixture was stirred for 20 minutes then iodomethane (1.1 mL, 18 mmol) was added dropwise with cooling in an ice bath. The resulting suspension was stirred at ambient temperature under a nitrogen atmosphere overnight. The reaction mixture was quenched with water (50 mL) then extracted with diethyl ether (150 mL). The organic layer was washed with water (5×50 mL), dried over magnesium sulfate then concentrated to provide 3.1 g of tert-butyl N-benzyloxy-N-methylcarbamate as a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05612377 |
| 출처 데이터셋 | uspto-grants-1997_03 |
| ORD ID | ord-3b5ac8a5b1854f79944972dfbdf8fb6b |
| 출처 메모 | uspto-grants-1997_03 |