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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221932Generated: October 31, 2026

Water → 2-(7-Hydroxymethyl-benzo[b]thiophen-3-yl)-ethanol

https://huagongshe.com/reaction/221932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 3-ethoxycarbonylmethyl-benzo[b]thiophene-7-carboxylateHCID 59488809—
SolventTetrahydrofuranHCID 8028—
Product2-(7-Hydroxymethyl-benzo[b]thiophen-3-yl)-ethanolHCID 5948879998%

Reaction Steps

Under a nitrogen stream, to a solution (38 mL) of lithium aluminum hydride (0.74 g, 19.5 mmol) in THF was added a solution (30 mL) of methyl 3-ethoxycarbonylmethyl-benzo[b]thiophene-7-carboxylate (2.7 g, 9.7 mmol) in THF at 0° C., and the resultant solution was stirred for 10 minutes at the same temperature. To the solution was further added lithium aluminum hydride (0.74 g, 19.5 mmol) at 0° C., and the resultant solution was stirred for 10 minutes at the same temperature. Ethyl acetate was added to the solution, and then water (5.2 mL) was added thereto at 0° C. The temperature of the resultant solution was raised to room temperature, and then the solution was stirred for 10 minutes. The reaction mixture was filtered through Celite. Solvent was then removed by distillation under reduced pressure. The resulting residue was treated by addition of ethyl acetate and n-hexane (1:2), to thereby obtain the titled compound (1.97 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207134B2
Source datasetuspto-grants-2012_06
ORD IDord-f07c633e182849bfb4fc1bd4762ba121
Source noteuspto-grants-2012_06