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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910088Generated: October 27, 2026

tert-Butanol → Benzo[b]thiophene-7-acetamide

https://huagongshe.com/reaction/910088

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzo[b]thiophene-7-acetonitrileHCID 11446611—
SolventEthyl AcetateHCID 8857—
ProductBenzo[b]thiophene-7-acetamideHCID 17985839—

Reaction Steps

Add benzo[b]thiophene-7-acetonitrile (1.9 g, 11.0 mmol) to 2-methyl-2-propanol (20 mL). Heat to reflux under nitrogen and add potassium hydroxide pellets (7.4 g, 132-mmol). Stir and reflux under nitrogen for 30 minutes. Pour solution off of the excess potassium hydroxide and dilute with ethyl acetate. Wash with a 1:1 mixture of aqueous saturated sodium chloride, aqueous saturated sodium hydrogen carbonate. Dry the organic phase over anhydrous magnesium sulfate, filter, and concentrate under reduced pressure. Rinse the solid with cold diethyl ether and dry under vacuum to obtain the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022065B2
Source datasetuspto-grants-2011_09
ORD IDord-fdfcf031fb1045af97bba0259b9722f6
Source noteuspto-grants-2011_09