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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620031Generated: November 4, 2026

N-bromobutanimide → HCID 66876970, compound

https://huagongshe.com/reaction/1620031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-(4-amino-2-methylphenyl)propanoateHCID 54187007—
SolventAcetonitrileHCID 6342—
ProductHCID 66876970HCID 6687697050.7%

Reaction Steps

A solution of Intermediate 8 (1.4 g) in acetonitrile (20 ml) was added with N-bromosuccinimide (1.4 g, WAKO) under ice cooling, stirred for 10 minutes under ice cooling, and then stirred at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure, then added with ethyl acetate (10 ml), and successively washed with saturated aqueous ammonium chloride, 5% aqueous sodium sulfite, saturated aqueous sodium hydrogencarbonate and saturated brine, the organic layer was dried, and then the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (Yamazen, n-hexane:ethyl acetate=3:1) to obtain the title compound (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772327B2
Source datasetuspto-grants-2014_07
ORD IDord-d927f99f03544f778b1867f30a03b04a
Source noteuspto-grants-2014_07