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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1714590생성일: 2026년 10월 25일

Water → 4-(3-Benzyloxyphenylthio)-2-chlorobenzaldehyde

https://huagongshe.com/reaction/1714590

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-4-fluorobenzaldehydeHCID 145024—
반응물3-(Benzyloxy)benzene-1-thiolHCID 24900601—
용매DimethylformamideHCID 6228—
생성물4-(3-Benzyloxyphenylthio)-2-chlorobenzaldehydeHCID 16655405—

반응 단계

3-Benzyloxybenzenethiol (13) (75.0 g, 347 mmol) and 2-chloro-4-fluorobenzaldehyde (55.0 g, 347 mmol) were dissolved in dimethylformamide (DMF) (350 mL) while the solution was being stirred. The solution was then placed in a water bath at 30° C. and potassium carbonate (62.3 g, 451 mmol) and dimethylformamide (25 mL) were added. This mixture was stirred for 30 min at an internal temperature of 40 to 42° C. Tap water (125 mL) was then added and the mixture was cooled in ice water. To the cooled mixture, additional tap water (625 mL) was added dropwise for crystallization. The mixture was stirred for 30 min and the resulting crystals were collected by filtration and washed with 10% aqueous 2-propanol (188 mL). The moist crystals were dissolved in ethyl acetate (750 mL) and the solution was washed twice with tap water (375 mL×2). The organic layer was concentrated under reduced pressure and acetone (900 mL) was added to the resulting residue. Purified water (386 mL) was then added dropwise at an internal temperature of 23° C. The mixture was stirred for 30 min and the resulting crystals were collected by filtration and washed with 50% aqueous acetone (400 mL). The washed crystals were air-dried overnight. Subsequently, the product was dried by blowing an air stream at 45° C. for 1 hour. This gave 4-(3-benzyloxyphenylthio)-2-chlorobenzaldehyde (1) as a colorless prism crystals (115 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07795472B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-3fbb0698e2ed4612868d175f61bf0fde
출처 메모uspto-grants-2010_09