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 | — |
| 반응물 | HCID 178418416 | HCID 178418416 | — |
| 촉매 | Triphenylphosphine | HCID 11776 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Tert-butyl (5-formyl-2-methoxybenzyl)carbamate | HCID 22493931 | 75.1% |
반응 단계
1.015 g of tertiary butyl N-(5-bromo-2-methoxybenzyl)carbamate, 45 mg of dichlorobis(triphenylphosphine) palladium (II), 330 mg of sodium formate and 17 mg of triphenyl phosphine were dissolved in anhydrous N,N-dimethylformamide and stirred at 110° C. for 2 hours in a carbon monoxide atmosphere. The reaction mixture was diluted with ethyl acetate, and successively washed with water and saturated aqueous sodium bicarbonate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evapoarated. The residue was purified by silica gel column chromatography, and from fractions eluted with hexane-ethyl acetate (3:1), 640 mg of tertiary butyl N-(5-formyl-2-methoxybenzyl)carbamate was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06884821B1 |
| 출처 데이터셋 | uspto-grants-2005_04 |
| ORD ID | ord-2a1a9a721a2944d49cd57c440706ca11 |
| 출처 메모 | uspto-grants-2005_04 |