Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → 6-Benzyloxymethyl-2-methyl-5,6-dihydro-4H-pyran-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Magnesium Bromide | HCID 82241 | — |
| 반응물 | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| 반응물 | 1,3-Bis (trimethylsilyloxy)butadiene | HCID 54494435 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-Benzyloxymethyl-2-methyl-5,6-dihydro-4H-pyran-4-one | HCID 19933042 | 60% |
반응 단계
A solution of 10.4 g of the aldehyde from Step 1 in 250 ml of THF was cooled to 0° C. and 1.0 eq. of freshly prepared MgBr2 was added dropwise. The mixture was warmed to r.t. and 40.6 g of 1,3-bis(trimethylsilyloxy)-1,3-butadiene (Emde, et al., Synthesis, p. 6 (1982)) was added. After 3 h., 50% aqueous HOAc was added and the mixture was stirred 10 min. and then extracted with Et2O (2x). After the ether was evaporated, the resultant oil was taken back up in 300 ml of CH2Cl2 and 12 ml of TFA. After 3 hours, the solution was washed with H2O, saturated NaHCO3, brine and finally dried over MgSO4. After flash chromatography, 9.5 g (60%) of the title compound was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05360815 |
| 출처 데이터셋 | uspto-grants-1994_11 |
| ORD ID | ord-4f201e79f89247afbe8108d2f96f8c54 |
| 출처 메모 | uspto-grants-1994_11 |