Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
tert-Butyldimethylsilyl chloride → Methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Methyl 2-hydroxy-6-methylbenzoate | HCID 584223 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoate | HCID 89705147 | 70.5% |
반응 단계
A mixture of methyl 2-hydroxy-6-methylbenzoate (prepared according to Doehner et al, WO 01/05739, 10.0 g), tert-butyldimethylsilyl chloride (11.0 g), N,N-di-isopropylethylamine (32 mL) and DMAP (0.75 g) in DCM (400 mL) was stirred at room temperature overnight. The mixture was washed with water and brine, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and pentane with a gradient of 0-10% to give methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoate (11.9 g) as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09440943B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-1ffebf94257d437d9795d4aab41dedd1 |
| 출처 메모 | uspto-grants-2016_09 |