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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908112Generated: October 24, 2026

Hydrochloric Acid → 4-(Isopropylthio)-3-methylbenzoic acid

https://huagongshe.com/en/reaction/1908112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Bromo-3-methylbenzoic acidHCID 82131—
ReactantIsopropyl propyl disulfideHCID 118529—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product4-(Isopropylthio)-3-methylbenzoic acidHCID 5855092634.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Butyllithium (16 mL of 1.6 M, 26 mmol) was added drop-wise to a mixture of 4-bromo-3-methyl-benzoic acid (2.5 g, 12 mmol) and THF (63 mL) at −78° C. The mixture was allowed to stir at −78° C. for 30 minutes before a solution of 2-isopropyldisulfanylpropane (1.7 g, 12 mmol) in THF (2 mL) was added drop-wise. The mixture was allowed to stir at −78° C. for 30 min, then 30 min at rt. The reaction mixture was then diluted with 100 mL of 1M aqueous sodium hydroxide. The organic layer was discarded and the aqueous layer was made acidic with 4M aqueous hydrochloric acid. The aqueous layer was then extracted 3 times with ethyl acetate. The combined extracts were dried over sodium sulfate and then evaporated to dryness. The crude material was purified by column chromatography using a gradient of 0-5% MeOH in dichloromethane to give 4-(isopropylthio)-3-methylbenzoic acid (870 mg, 18%). MS m/z calc. 210.3. found 211.2 (M+1)+. Retention time: 2.32 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-15b5c7efc57445d69a13ce7d01647e70
Source noteuspto-grants-2013_12