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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638940Generated: October 31, 2026

Potassium Hydroxide → 3,5-bis-dimethylthiocarbamoyloxybenzoic acid methyl ester

https://huagongshe.com/reaction/638940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
ReactantMethyl 3,5-DihydroxybenzoateHCID 75076—
SolventDimethylformamideHCID 6228—
Product3,5-bis-dimethylthiocarbamoyloxybenzoic acid methyl esterHCID 1213834863.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3,5-dihydroxybenzoic acid methyl ester (10.0 g, 59.5 mmol) in DMF (200 mL) at 0° C. was added NaH (60% dispersion in mineral oil, 5.00 g, 125 mmol, 2.1 eq.) in small portions. The reaction mixture was stirred at 0° C. for 15 min then warmed to room temperature. After 1 h, the reaction mixture was cooled to 0° C. and then added dimethylthiocarbamoyl chloride (14.7 g, 119 mmol). Following the addition, the reaction was stirred for 45 min at 0° C., then for 30 min at room temperature and then heated to 80° C. After 2 h at 80° C., the reaction mixture was cooled to room temperature and then added to 1% aqueous KOH (500 mL). The resulting mixture was extracted with ethyl ether (2×500 mL). The organic layer was washed with H2O (500 mL), brine (300 mL), dried over MgSO4 and concentrated in vacuo to afford 3,5-bis-dimethylthiocarbamoyloxybenzoic acid methyl ester (13.0 g). This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691843B2
Source datasetuspto-grants-2010_04
ORD IDord-f61fe97ace3247e383b854a5e2a40399
Source noteuspto-grants-2010_04