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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247676Generated: October 30, 2026

Water → (4-Ethynyl-2-thienyl)methanol

https://huagongshe.com/reaction/2247676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Ethynylthiophene-2-carbaldehydeHCID 51345981—
SolventMethanolHCID 887—
Product(4-Ethynyl-2-thienyl)methanolHCID 8662021860%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-ethynylthiophene-2-carboxaldehyde (1.5 g, 11 mmol) that was obtained in Example 9 (9b) in methanol (30 ml) was added sodium borohydride (0.49 g, 13 mmol) at 0° C. with stirring, and then the resulting mixture was stirred at room temperature for 15 minutes. After cooling the reaction mixture to 0° C., water (100 ml) was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:9 to 3:7) as the eluent to afford the title compound (0.88 g) in a yield of 60% as a brown oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-3f3295ce5b63415db99afff402aa9ad7
Source noteuspto-grants-2010_03