戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 39328作成日:2026年10月26日

Chlorodifluoromethane → 4-(Difluoromethoxy)-3-hydroxybenzaldehyde

https://huagongshe.com/reaction/39328

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorodifluoromethaneHCID 6372—
反応物3,4-DihydroxybenzaldehydeHCID 8768—
反応物Potassium CarbonateHCID 11430—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-(Difluoromethoxy)-3-hydroxybenzaldehydeHCID 275829525%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524905B2
出典データセットuspto-grants-2013_09
ORD IDord-ac21ed1fc5ba469eb3bf2c9a44f79dad
出典メモuspto-grants-2013_09