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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183629Generated: October 31, 2026

2-Chloro-N-methoxy-N-methylacetamide → HCID 22473705, compound

https://huagongshe.com/reaction/2183629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N-methoxy-N-methylacetamideHCID 2734716—
ReactantHCID 22473703HCID 22473703—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22473705HCID 2247370597.1%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 3-bromo-4-methylbenzo[b]thiophene (2 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; 4.58 ml) in ether (30 ml), then the mixture was stirred at −70° C. for 30 minutes. A solution of 2-chloro-N-methoxy-N-methylacetamide (1.04 g) in tetrahydrofuran (10 ml) was added dropwise at −70° C. over 10 minutes, then the mixture was stirred at −70° C. for 5 hours, allowed to stand at ambient temperature for 18 hours and quenched by the addition of saturated aqueous ammonium chloride solution (40 ml). The organic layer was separated, washed with saturated aqueous sodium chloride solution (40 ml), and dried (MgSO4). The solvents were removed in vacuo to give 2-chloro-1-(4-methylbenzo[b]thiophen-2-yl]ethan-1-one (1.65 g) as a brown oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-16932680358547ec8d79f0ca05a7577f
Source noteuspto-grants-2005_05