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HRID 745805作成日:2026年10月27日

Benzenesulfinyl chloride → 5-Phenylsulphinyl-6-methyl-1,3-benzodioxole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/745805

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfinyl chlorideHCID 4190003—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物5-Methyl-1,3-benzodioxole-2-carboxylic acid ethyl esterHCID 54313136—
溶媒1,2-DichloroethaneHCID 11—
溶媒1,1-DichloroethaneHCID 6365—
生成物5-Phenylsulphinyl-6-methyl-1,3-benzodioxole-2-carboxylic acid ethyl esterHCID 54259655—

反応手順

20.8 g (0.1 mol) of 5-methyl-1,3-benzodioxole-2-carboxylic acid ethyl ester Example 2b) and 19.2 g (0.125 mol) of phenylsulphinic acid chloride are dissolved in 200 ml of 1,2-dichloroethane and cooled to 5° using an ice-bath. 13.3 g (0.1 mol) of aluminium chloride are introduced in the course of approximately 15 minutes at from 5°-10° while stirring. The mixture is stirred for a further hour in the ice-bath and is then poured out onto ice-water. The resulting emulsion is diluted with 200 ml of dichloroethane and filtered across a layer of a filter aid (for example Hyflo). The filtrate is introduced into a separating funnel and the layers are separated. The organic phase is dried over sodium sulphate, filtered and concentrated to dryness by evaporation. A light brown honey-like product, 5-phenylsulphinyl-6-methyl-1,3-benzodioxole-2-carboxylic acid ethyl ester, is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04600709
出典データセットuspto-grants-1986_07
ORD IDord-3626516582ce4e578fbdc7089df2579f
出典メモuspto-grants-1986_07