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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274927Generated: October 27, 2026

N-bromobutanimide → Methyl 2-(1,3-benzodioxol-5-yl)-2-bromoacetate

https://huagongshe.com/reaction/274927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-(1,3-dioxaindan-5-yl)acetateHCID 266588—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-(1,3-benzodioxol-5-yl)-2-bromoacetateHCID 11821769—

Reaction Steps

N-Bromosuccinimide (3.95 g, 22.2 mmol) and AlBN (0.098 g, 0.06 mMol) were added to a solution of methyl (3,4-methylenedioxyphenyl)acetate (3.9 g, 21.2 mmol) in carbon tetrachloride and the mixture was refluxed for 2.5 h. The reaction was cooled and filtered. The flitrate was concentrated in vacuo and the residue obtained was purified by flash chromatography on silica-gel using 10% ethyl acetate-hexane. Yield 2.6 g (oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391566
Source datasetuspto-grants-1995_02
ORD IDord-a9cf8f7d1d0a4ed0a7d2735fe2105d2e
Source noteuspto-grants-1995_02