돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893165생성일: 2026년 10월 27일

Butyl methyl ether → Ethyl 3-[4-(benzyloxy)phenyl]-2-ethoxyprop-2-enoate

https://huagongshe.com/reaction/1893165

반응식

참여 물질

역할이름HCID투입량
반응물Butyl methyl etherHCID 12338—
반응물Triethyl phosphiteHCID 31215—
반응물Benzaldehyde, 4-(phenylmethoxy)-HCID 78109—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물Ethyl 3-[4-(benzyloxy)phenyl]-2-ethoxyprop-2-enoateHCID 5442385492%

반응 단계

P(OEt)3 was added dropwise to a mixture of tent-butyl methyl ether 55 mL) and potassium tert-butoxide (4.65 g, 41.4 mmol) under a nitrogen atmosphere at 20-30° C. 4-Benzyloxybenzaldehyde (4.61 g, 21.7 mmol) was added in portions to this mixture at 5° C. followed by the addition of tert-butyl alcohol (6.70 g). The reaction mixture was allowed to reach 15° C. and stirred at this temperature for approximately 30 min, after which the reaction was completed (as judged by TLC). Water (30 mL) was added at 5-10° C., and the phases were allowed to separate. The organic phase was concentrated in vacuo, and ethanol (30 mL) was added to the stirred solution. After crystallization had occurred, water (18 mL) was added to the suspension. The light-yellow title compound was filtered off, washed with ethanol/water (1:1 v/v), and dried in vacuo to yield 6.52 g (92% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513233B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-61d528ca74cd4b48a02921468bcf1878
출처 메모uspto-grants-2013_08