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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397823생성일: 2026년 10월 24일

Phenoxyacetaldehyde → 2-Phenoxymethyl-2,3-dihydropyran-4-one

https://huagongshe.com/ko/reaction/397823

반응식

참여 물질

역할이름HCID투입량
반응물PhenoxyacetaldehydeHCID 75033—
반응물1-Methoxy-3-trimethylsilyloxy-1,3-butadieneHCID 101051—
촉매ZincchlorideHCID 3007855—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물2-Phenoxymethyl-2,3-dihydropyran-4-oneHCID 2300126644.4%

반응 조건

온도-5 °C

반응 단계

1-Methoxy-3-(trimethylsilyloxy)-1,3-butadiene (4.95 ml; 26 mmol) was added to a solution of phenoxyacetaldehyde (3.56 g, 26 mmol) in DCM (40 ml). The solution was cooled to −5° C. A 2.3 M solution of zinc chloride in DCM (5.6 ml, 13 mmol) was added. The reaction mixture was stirred for 16 hours, while it was warming up to room temperature. It was diluted with ethyl acetate (150 ml) and washed with a 10% aqueous solution of sodium hydrogensulphate (100 ml). The aqueous phase was extracted with ethyl acetate (100 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (200 g), using ethyl acetate/heptane (1:1) as eluent, to give 2.36 g of 2-phenoxymethyl-2,3-dihydropyran-4-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610721B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-accf40c1ec45459c972fdbb8ac03c32c
출처 메모uspto-grants-2003_08