Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183636Generated: October 31, 2026

N-Methoxy-N-methylpropionamide → HCID 22473751, compound

https://huagongshe.com/reaction/2183636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylpropionamideHCID 11344007—
ReactantHCID 22473703HCID 22473703—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22473751HCID 2247375134.9%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 3-bromo-4-methylbenzo[b]thiophene (1.69 g) in tetrahydrofuran (10 ml) was added dropwise under nitrogen at −70° C. over 10 minutes to a stirred solution of n-butyllithium (2.5M solution in hexanes; 3.87 ml) in ether (30 ml), then the mixture was stirred at −70° C. for 30 minutes. A solution of N-methoxy-N-methylpropionamide (1.31 g) in tetrahydrofuran (10 ml) was added dropwise at −70° C. over 10 minutes, the mixture was stirred at −70° C. for 3 hours, then it was allowed to warm to ambient temperature and quenched by the addition of saturated aqueous ammonium chloride solution (30 ml). The organic layer was separated, washed with saturated aqueous sodium chloride solution (30 ml), and dried (MgSO4). The solvents were removed in vacuao to give 1-(4-methylbenzo[b]thiophen-2-yl)propan-1-one (0.53 g) as an orange solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-aa8be48533d54085a1117758a789f9cb
Source noteuspto-grants-2005_05