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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467459Generated: October 25, 2026

Acetic Anhydride → N-(1-(4-bromophenyl)propan-2-yl)acetamide

https://huagongshe.com/reaction/467459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Bromo-alpha-methylbenzeneethanamineHCID 205668—
SolventAcetic AcidHCID 176—
ProductN-(1-(4-bromophenyl)propan-2-yl)acetamideHCID 45824256—

Reaction Steps

17.0 mL (179.7 mmol) acetic anhydride are added to a mixture of 24.2 g (113 mmol) 1-(4-bromophenyl)propane-2-amine and 20 mL AcOH and the reaction mixture is stirred at r.t. over night. The solvent is evaporated in vacuo, and the residue partitonated between TBME and a saturated aq. NaHCO3 solution. The layers are separated and the organic layer is washed with water, dried with Na2SO4, filtered and the solvent is removed in vacuo. The crude product is triturated with DIPE.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623860B2
Source datasetuspto-grants-2014_01
ORD IDord-5ed5faccfa8741a89d4252efa52b52aa
Source noteuspto-grants-2014_01