Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Methylbenzaldehyde → Ethyl 3-methylcinnamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Methylbenzaldehyde | HCID 12105 | — |
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| 반응물 | Ethyl [bis(2,2,2-trifluoroethoxy)phosphinyl]acetate | HCID 11759356 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 3-methylcinnamate | HCID 589327 | — |
반응 단계
KHMDS (4.0 g, 20.0 mmol) was added to a solution of ethyl[bis(2,2,2-trifluoro-ethoxy)phosphinyl]acetate (4.7 mL, 20.0 mmol) and 18-crown-6 (10.6 g, 40.0 mmol) in THF (200 mL) at −78° C., and stirred for 30 minutes. m-Tolualdehyde (2.1 mL, 18 mmol) was added and the reaction mixture was stirred for 3 hours from −78° C. to room temperature. The reaction was quenched with aqueous hydrochloric acid (1M solution, 100 mL), and the product was extracted with EtOAc (3×100 mL). The organic extracts were washed with brine (100 mL), dried over MgSO4, and concentrated to afford the subtitle compound, which was used without further purification. MS calculated for C12H14O2+H: 191, observed: 191.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09096520B2 |
| 출처 데이터셋 | uspto-grants-2015_08 |
| ORD ID | ord-47abcb40a91743f0a13cae85f03f56f8 |
| 출처 메모 | uspto-grants-2015_08 |