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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477325Generated: October 26, 2026

Sodium methanethiolate → 2,2-Dimethyl-5-[2-(methylthio)acetyl]-1,3-benzodioxole

https://huagongshe.com/reaction/477325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant2-Bromo-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)ethanoneHCID 14373073—
Reactantalpha-MethylthioacetophenoneHCID 18968240—
SolventMethanolHCID 887—
Product2,2-Dimethyl-5-[2-(methylthio)acetyl]-1,3-benzodioxoleHCID 14373074—

Reaction Steps

The procedure is as in Example 4 for the preparation of α-methylthioacetophenone, starting with a stirred solution of 5-(2-bromoacetyl)-2,2-dimethyl-1,3-benzodioxole (14.9 g) in methanol (150 cc). Sodium methanethiolate (3.8 g) is added in the course of 5 minutes at a temperature in the region of 20° C., and the mixture is left with stirring for 15 hours at the same temperature. 2,2-Dimethyl-5-[2-(methylthio)acetyl]-1,3-benzodioxole (11 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886835
Source datasetuspto-grants-1989_12
ORD IDord-fcb6d5b3eb434a7597996d1bdf9306cf
Source noteuspto-grants-1989_12