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HRID 1390597作成日:2026年10月25日

1-Butanol → 2-(Bromomethyl)-4-(4-chloro-1-naphthalenyloxymethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolane

https://huagongshe.com/reaction/1390597

反応式

関与物質

役割名称HCID仕込み量
反応物1-ButanolHCID 263—
反応物p-Toluenesulfonic acidHCID 6101—
反応物2-Bromo-1-(2,4-dichlorophenyl)ethan-1-oneHCID 75828—
反応物3-(4-Chloro-1-naphthalenyloxy)-1,2-propanediolHCID 20332658—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物2-(Bromomethyl)-4-(4-chloro-1-naphthalenyloxymethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolaneHCID 20332695—

反応手順

A mixture of 13.6 parts of 2-bromo-1-(2,4-dichlorophenyl)-1-ethanone, 15.2 parts of 3-(4-chloro-1-naphthalenyloxy)-1,2-propanediol, 3 parts of 4-methylbenzenesulfonic acid, 80 parts of butanol and 180 parts of benzene is stirred and refluxed for 24 hours with water-separator. The reaction mixture is evaporated and the residue is triturated in 2-propanol. The product is filtered off and crystallized from butanol, yielding A + B 2-(bromomethyl)-4-(4-chloro-1-naphthalenyloxymethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolane; mp. 122.7° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04139540
出典データセットuspto-grants-1979_02
ORD IDord-8551beb4778242b4b91124191fc3952a
出典メモuspto-grants-1979_02