HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745805Generated: October 25, 2026
Benzenesulfinyl chloride → HCID 54259655, compound
https://huagongshe.com/reaction/745805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfinyl chloride | HCID 4190003 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Methyl-1,3-benzodioxole-2-carboxylic acid ethyl ester | HCID 54313136 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 54259655 | HCID 54259655 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04600709 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-3626516582ce4e578fbdc7089df2579f |
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| Source note | uspto-grants-1986_07 |
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