Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Formate → Tert-butyl (5-formyl-2-methoxybenzyl)carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Formate | HCID 2723810 | — |
| 반응물 | Tert-butyl (5-bromo-2-methoxybenzyl)carbamate | HCID 22926030 | — |
| 촉매 | Triphenylphosphine | HCID 11776 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | HCID 178418416 | HCID 178418416 | — |
| 생성물 | Tert-butyl (5-formyl-2-methoxybenzyl)carbamate | HCID 22493931 | 75.1% |
반응 단계
1.015 g of t-butyl N-(5-bromo-2-methoxybenzyl)carbamate, 45 mg of dichlorobis(triphenylphosphine)palladium (II), 330 mg of sodium formate and 17 mg of triphenylphosphine were dissolved in anhydrous N,N-dimethylformamide, followed by stirring for 2 hours at 110° C. in carbon monoxide atmosphere. The reaction mixture was diluted with ethyl acetate, and washed with water and saturated sodium bicarbonate water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography, and 640 mg of t-butyl N-(5-formyl-2-methoxybenzyl)carbamate was obtained from fractions eluted with hexane-ethyl acetate (3:1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07244861B2 |
| 출처 데이터셋 | uspto-grants-2007_07 |
| ORD ID | ord-04a0c5bca7cd4ea2a1e72ff93846ae5a |
| 출처 메모 | uspto-grants-2007_07 |