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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737441Generated: October 31, 2026

Dimethylformamide → diazomethyl-(2-(S)-(3,4-dichlorophenyl)-pent-4-en-yl)-ketone

https://huagongshe.com/reaction/1737441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiazomethaneHCID 9550—
ReactantOxalyl chlorideHCID 65578—
Reactant(S)-2-(3,4-dichlorophenyl)pent-4-enoic acidHCID 15261879—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Productdiazomethyl-(2-(S)-(3,4-dichlorophenyl)-pent-4-en-yl)-ketoneHCID 5428556084%

Reaction Steps

To a solution of 2-(S)-(3,4-dichlorophenyl)-pent-4-enoic acid (5.04 g, 20.6 mmol) in 60 mL of dichloromethane was added oxalyl chloride 2.15 mL (24.6mmol) and dimethylformamide (0.1 mL) upon cooling in an ice-water bath. The cooling bath was then removed and the reaction mixture was stirred at rt overnight. The solvent was removed under reduced pressure. The resulting material was diluted in ethyl acetate and concentrated in vacuo in order to remove residual HCl. The residual crude acid chloride was dissolved in 70 mL of ether and was slowly added to a 100 mL ether solution of diazomethane (77 mmol). After stirring for 2 hr at rt, the solvent was removed under vacuum. The resulting yellow oil was chromatographed on silica gel column eluting with a gradient of hexane:ethyl acetate=20:1 to 3:1 to give 4.66g (84%) of diazomethyl-(2-(S)-(3,4-dichlorophenyl)-pent-4-en-yl)-ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962462
Source datasetuspto-grants-1999_10
ORD IDord-ff0e7537c6eb4bafa17ad0c0598a58f6
Source noteuspto-grants-1999_10