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HRID 1648889作成日:2026年10月26日

Hydrochloric Acid → (4,5-Dimethoxy-2-fluorophenyl)-phenylmethanone

https://huagongshe.com/reaction/1648889

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzoyl chlorideHCID 7412—
反応物4-Fluoro-1,2-dimethoxybenzeneHCID 593640—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒1,2-DichloroethaneHCID 11—
生成物(4,5-Dimethoxy-2-fluorophenyl)-phenylmethanoneHCID 20396992—

反応手順

12.7 g (95 mmol) of aluminium trichloride in 80 ml of 1,2-dichloroethane are stirred under nitrogen and cooled to 3°. 13.35 g (95 mmol) of benzoyl chloride are added. At 3°, this red solution is added dropwise over a period of 25 minutes to a solution of 12.55 g (80.3 mmol) of 1,2-dimethoxy-4-fluorobenzene (4-fluoroveratrole) in 80 ml of 1,2-dichloroethane. The reaction mixture is stirred for a further 3 hours at 3°, then for 31/2 hours at room temperature and then poured onto a mixture of 250 ml of ice and 20 ml of concentrated hydrochloric acid. The organic phase is separated off and the aqueous phase is extracted several times with ether. Organic phase and ether solutions are combined, washed with 1 N sodium hydroxide solution, water and with saturated sodium chloride solution, dried over magnesium sulphate and concentrated by evaporation. The resulting yellow oil is stirred with 50 ml of ether in an ice bath until crystallisation takes place, yielding the desired (4,5-dimethoxy-2-fluorophenyl)-phenylmethanone in the form of white crystals having a melting point of 102°-103°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04414214
出典データセットuspto-grants-1983_11
ORD IDord-5bd321c7a9584b8fa26ab361b018d2aa
出典メモuspto-grants-1983_11