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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502942Generated: November 4, 2026

Hydrochloric Acid → (3-Chloro-4-methylthiophen-2-yl)methanol

https://huagongshe.com/reaction/502942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 3-chloro-4-methylthiophene-2-carboxylateHCID 2777567—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(3-Chloro-4-methylthiophen-2-yl)methanolHCID 5976769792.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Lithium aluminum hydride (1.35 g) was added to a THF (50 ml) solution of methyl 3-chloro-4-methylthiophene-2-carboxylate (3.40 g) at 0° C., followed by stirring at 0° C. for 20 minutes. An 1M aqueous hydrochloric acid solution was added to the reaction solution and the whole was stirred at room temperature for 1 hour. The solution was filtered and, after ethyl acetate was added, the organic layer was separated. Furthermore, the organic layer washed with brine and, after drying over anhydrous sodium sulfate and filtration, the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by column chromatography (hexane:ethyl acetate=4:1) to obtain 2.68 g of (3-chloro-4-methyl-2-thienyl)methanol (pale yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776897B2
Source datasetuspto-grants-2010_08
ORD IDord-10c891dbc6f84eb99077cbf9ea87afca
Source noteuspto-grants-2010_08