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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357773Generated: October 29, 2026

Sodium Thiosulfate → Ethyl 5-chloro-4-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/357773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSulfuryl chlorideHCID 24648—
ReactantEthyl 4-methylthiophene-2-carboxylateHCID 18973097—
SolventAcetonitrileHCID 6342—
ProductEthyl 5-chloro-4-methylthiophene-2-carboxylateHCID 12605958—

Reaction Steps

4-Methyl-2-thiophenecarboxylic acid ethyl ester (3.4 g) synthesized in accordance with the method of Reference Example 140 was dissolved in acetonitrile (30 ml), and sulfuryl chloride (2.4 ml) in acetonitrile (20 ml) was added dropwise. The mixture was stirred at room-temperature for 30 minutes, and 10% aqueous sodium thiosulfate (100 ml) was added. The mixture was stirred at room temperature for 2 hours and extracted with diethyl ether. The extract was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography, and the desired fractions were concentrated under reduced pressure to give 5-chloro-4-methyl-2-thiophenecarboxylic acid ethyl ester (4.09 g). 5-Chloro-4-methyl-2-thiophenecarboxylic acid ethyl ester (4.09 g) was dissolved in a mixture of ethanol (20 ml) and tetrahydrofuran (20 ml), and 1N aqueous sodium hydroxide (40 ml) was added. The mixture was stirred at 60° C for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 5-chloro-4-methyl-2-thiophenecarboxylic acid (2.37 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840917
Source datasetuspto-grants-1998_11
ORD IDord-6d570ac0959b40c0a15d80fb02a664b7
Source noteuspto-grants-1998_11