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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39328생성일: 2026년 10월 24일

Chlorodifluoromethane → 4-(Difluoromethoxy)-3-hydroxybenzaldehyde

https://huagongshe.com/ko/reaction/39328

반응식

참여 물질

역할이름HCID투입량
반응물ChlorodifluoromethaneHCID 6372—
반응물3,4-DihydroxybenzaldehydeHCID 8768—
반응물Potassium CarbonateHCID 11430—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-(Difluoromethoxy)-3-hydroxybenzaldehydeHCID 275829525%

반응 단계

To a well stirred suspension of 3,4-dihydroxy benzaldehyde (100 gm) and anhydrous potassium carbonate (120 gm) in dry N,N-dimethylformamide (1.0 lit) was passed chlorodifluoromethane gas for about 30 minutes at about 80-85° C. After an hour another lot of anhydrous potassium carbonate (25.0 gm) was added and stirred for about one and half hours. The third lot of anhydrous potassium carbonate (25.0 gm) was added and stirred for about one and half hours. The reaction mixture was then stirred for about 5-6 hours at an ambient temperature. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue obtained was diluted with water (500 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude product obtained was purified through silica gel column to give 4-difluoromethoxy-3-hydroxy benzaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524905B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ac21ed1fc5ba469eb3bf2c9a44f79dad
출처 메모uspto-grants-2013_09