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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171228Generated: October 27, 2026

Water → (6-Methoxy-benzo[b]thiophen-2-yl)-methanol

https://huagongshe.com/reaction/1171228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 6-methoxybenzo[b]thiophene-2-carboxylateHCID 11831419—
ReactantAluminium lithium hydrideHCID 21226445—
SolventEthyl AcetateHCID 8857—
Product(6-Methoxy-benzo[b]thiophen-2-yl)-methanolHCID 57608293100%

Reaction Steps

To a tetrahydrofuran (100 mL) solution of (6-methoxy-benzo[b]-thiophene-2-carboxylic acid ethyl ester (5.0 g, 21.1 mmol) described in Production Example 77-1-1 was added lithium aluminum hydride (2.0 g, 52.8 mmol). The suspension was stirred at room temperature for 30 minutes. The reaction mixture was distributed between water and ethyl acetate. The organic layer was separated followed by drying over anhydrous magnesium sulfate and filtering. The residue was concentrated under a reduced pressure to obtain the title compound (4.1 g, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829585B2
Source datasetuspto-grants-2010_11
ORD IDord-6644c6f6b7314d86b60111c5209d7b17
Source noteuspto-grants-2010_11