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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977354Generated: October 25, 2026

Allyl bromide → 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester

https://huagongshe.com/reaction/1977354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(N-methyl-hydroxycarbamoyl)-5-nitro-benzoic acid allyl esterHCID 22986101—
SolventDimethylformamideHCID 6228—
Product3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl esterHCID 2298610083.3%

Reaction Steps

A mixture of (8(a)) (0.60 g), allyl bromide (0.28 g), potassium carbonate (0.59 g) and DMF (20 ml) was stirred for 3 hours at ambient temperature under an argon atmosphere. The dimethyl formamide was then evaporated under reduced pressure and the residue dissolved in ethyl acetate (50 ml) and water (50 ml). The organic phase was separated, washed with brine (50 ml), dried over magnesium sulphate and evaporated under reduced pressure to dryness to give 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester (8(b)) as a yellow oil (0.571 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232338B1
Source datasetuspto-grants-2001_05
ORD IDord-793cee6126f848ceb335d8fb4c0a33b6
Source noteuspto-grants-2001_05