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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183601Generated: October 30, 2026

Benzo(B)Thiophene → 1-Benzo[b]thien-2-yl-1-propanone

https://huagongshe.com/reaction/2183601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-Methoxy-N-methylpropionamideHCID 11344007—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product1-Benzo[b]thien-2-yl-1-propanoneHCID 2247421380.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (1.6 M solution in hexanes; 28.9 ml) was added dropwise under nitrogen at 0° C. to a stirred solution of benzo[b]thiophene (6.21 g) in ether (90 ml), then the mixture was stirred 0° C. for 15 minutes and cooled to −70° C. A solution of N-methoxy-N-methylpropionamide (5.42 g) in ether (40 ml) was added over 10 minutes, then the mixture was allowed to warm to ambient temperature and was stirred at ambient temperature for 3.5 hours. The mixture was poured into saturated aqueous ammonium chloride solution (200 ml) and ethyl acetate (100 ml) and water (50 ml) were added. The organic phase was separated, washed with saturated aqueous sodium chloride solution (150 ml), dried (Na2SO4) and the solvents were removed in vacua. The residue was triturated with petroleum ether (b.p. 40-60° C.) (25 ml) and the resulting solid was collected by filtration and dried in vacuo to give 1-(benzo[b]thiophen-2-yl)propan-1-one (7.05 g) as a colourless solid, m.p. 79-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-fdcbc5da3ff945e88f44e5aa4bc764fe
Source noteuspto-grants-2005_05