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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849555Generated: October 31, 2026

N-Methoxy-N-methyl-(2S)-(3,4-dichlorophenyl)-4-pentenamide → 3-(S)-(3,4-dichlorophenyl)-5-hexen-2-one

https://huagongshe.com/reaction/849555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methyl-(2S)-(3,4-dichlorophenyl)-4-pentenamideHCID 18392767—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product3-(S)-(3,4-dichlorophenyl)-5-hexen-2-oneHCID 1839275593%

Reaction Steps

A solution of 319 mg (1.11 mmoL) of N-methoxy-N-methyl-2-(S)-(3,4-dichlorophenyl)-4-pentenamide (from Step 1 above) in 10 mL of dry tetrahydrofuran was cooled to -70° C. and treated with 1.0 mL (1.40 mmol) of methyllithium and stirred between -70° C. to -40° C. After 3 hours, the reaction was quenched with 5 mL of water, and diluted with 10 mL of ethyl acetate. The layers were separated and the organic layer was washed with water (3×10 mL). The aqueous layers were extracted with 10 mL of ethyl acetate. The combined organic layers were washed with 10 mL of saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography on 44 g of silica gel using 1:3 v/v ethyl acetate/hexane as the eluant afforded 250 mg (93%) of the title compound as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06013652
Source datasetuspto-grants-2000_01
ORD IDord-f27bd012310044038317d85937930a47
Source noteuspto-grants-2000_01