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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944490Generated: October 29, 2026

Toluene → (3,4-Dichloroisothiazol-5-yl)methanol

https://huagongshe.com/reaction/1944490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
Reactant3,4-Dichloro-5-isothiazolecarboxylic acidHCID 49837—
SolventDimethylformamideHCID 6228—
Product(3,4-Dichloroisothiazol-5-yl)methanolHCID 1672316659.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3,4-dichloroisothiazole-5-carboxylic acid (2.0 g) and toluene (20 mL) was treated with thionyl chloride (5.0 mL) and N,N-dimethylformamide (0.5 mL), and the resulting mixture was heated at 100° C. for 16 hours. The mixture was concentrated under reduced pressure and the residue was dissolved in tetrahydrofuran (5.0 mL). The mixture was cooled to −78° C. and treated dropwise over a period of 1 hour with a 2.0 M solution of sodium borohydride in N,N-dimethylformamide (8.5 mL). The mixture was stirred at −78° C. for 5 minutes, diluted with 1.0 M aqueous hydrochloric acid solution and extracted with ethyl acetate. The combined organic extract was washed with saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with a mixture of cyclohexane and dichloromethane (1:0 to 0:1 by volume) to afford the title compound as a pale yellow solid (1.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394836B2
Source datasetuspto-grants-2013_03
ORD IDord-e0db55158c1c439b802d8b5b3a1f3c86
Source noteuspto-grants-2013_03