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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267460Generated: October 31, 2026

Diisopropylamine → 6-Methoxybenzo[B]thiophen-3(2H)-one

https://huagongshe.com/reaction/2267460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantN,N-Diethyl-4-methoxy-2-(methylthio)benzamideHCID 57428875—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxybenzo[B]thiophen-3(2H)-oneHCID 12101625—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-BuLi (1.6 M in hexanes, 13 mL, 20.8 mmol) was added slowly to a solution of diisopropylamine (2.91 mL, 20.8 mmol) in THF at −78° C. The mixture was stirred under nitrogen for 30 min and N,N-diethyl-4-methoxy-2-(methylthio)benzamide (2.4 g, 9.47 mmol), dissolved in 10 mL of anhydrous THF was added to the reaction dropwise. Stirring was continued at −78° C. for 1 h and the cooling bath was removed. After 12 h, the reaction was cooled back down to −78° C. and a 1:1 mixture of methanol and acetic acid (10 mL) was added to the mixture. The reaction was stirred for 15 min and the cooling bath was removed and allowed to warm up to room temperature. The reaction was diluted with ethyl acetate and the organic layer was washed with saturated aqueous sodium bicarbonate, water and brine. The organic layer was then dried with sodium sulfate, concentrated and purified by flash chromatography using a gradient of 15 to 40% ethyl acetate in hexanes to obtain an off white solid. Yield=1.4 g. MS (M−H)-179.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-e14a89f540914083af654924ed783bb5
Source noteuspto-grants-2010_12