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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652646Generated: October 30, 2026

2-Bromoisovaleric acid → 2-[(2,3-Dichloro-4-methoxyphenyl)sulfanyl]-3-methylbutanoic acid

https://huagongshe.com/reaction/652646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoisovaleric acidHCID 11268—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dichloro-4-methoxybenzene-1-thiolHCID 15914269—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[(2,3-Dichloro-4-methoxyphenyl)sulfanyl]-3-methylbutanoic acidHCID 1591427080.5%

Reaction Steps

To 3.13 g of 99% sodium hydride under nitrogen at room temperature is added a solution of 12.26 g of 2,3-dichloro-4-methoxythiophenol in 100 ml of sieve-dried dimethylformamide over 2 minutes. The reaction is stirred for 12 minutes. A solution of 9.56 g of α-bromoisovaleric acid in 85 ml of dimethylformamide is added over 4 minutes. The reaction is stirred at room temperature for 3 hours, cooled in ice, diluted with 500 ml of water and filtered. The solution is cooled and acidified with 3N hydrochloric acid to give the product. The precipitate is filtered, washed with a small amount of water, dried and recrystallized from acetone-pentane to give 13.14 g of α-(2,3-dichloro-4-methoxyphenylthio)isovaleric acid as a white crystalline powder mp 176.5°-178.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04672138
Source datasetuspto-grants-1987_06
ORD IDord-15ddc7cfaa5c4d009c0a7e46ed5ef4a4
Source noteuspto-grants-1987_06