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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747033Generated: October 25, 2026

Hydrochloric Acid → Methyl 5-(hydroxymethyl)thiophene-3-carboxylate

https://huagongshe.com/reaction/1747033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 5-formylthiophene-3-carboxylateHCID 818925—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductMethyl 5-(hydroxymethyl)thiophene-3-carboxylateHCID 1292649896.1%

Reaction Steps

To a mixed liquid of 5.00 g of methyl 5-formylthiophene-3-carboxylate and 50 ml of THF was added 0.67 g of sodium borohydride under ice-cooling. To the reaction solution was added dropwise 5 ml of methanol, followed by stirring for 1 hour under ice-cooling. The reaction solution was added with 1 M hydrochloric acid, extracted with ethyl acetate, and washed with a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and the solvent was then evaporated to obtain 4.86 g of methyl 5-(hydroxymethyl)thiophene-3-carboxylate as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150541B2
Source datasetuspto-grants-2015_10
ORD IDord-52c269d4da2641efb3b4e1b72ca6d577
Source noteuspto-grants-2015_10