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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2379169생성일: 2026년 10월 26일

Acetic Acid → 6-Benzyloxymethyl-2-methyl-5,6-dihydro-4H-pyran-4-one

https://huagongshe.com/reaction/2379169

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Magnesium BromideHCID 82241—
반응물(Phenylmethoxy)acetaldehydeHCID 108989—
반응물1,3-Bis (trimethylsilyloxy)butadieneHCID 54494435—
용매TetrahydrofuranHCID 8028—
생성물6-Benzyloxymethyl-2-methyl-5,6-dihydro-4H-pyran-4-oneHCID 1993304260%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05360815
출처 데이터셋uspto-grants-1994_11
ORD IDord-4f201e79f89247afbe8108d2f96f8c54
출처 메모uspto-grants-1994_11