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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602383Generated: October 31, 2026

N-bromobutanimide → 3-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propylamine

https://huagongshe.com/reaction/1602383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-(2,3-Dihydro-benzofuran-4-yl)-propylamine hydrochlorideHCID 19611670—
SolventAcetic AcidHCID 176—
Product3-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propylamineHCID 19611637—

Reaction Steps

A solution of the free base (200 mg) liberated from 3-(2,3-dihydro-benzofuran-4-yl)-propylamine hydrochloride and N-bromosuccinimide (215 mg) in acetic acid (5 ml) was stirred at room temperature overnight. The solution was evaporated to dryness and the residue taken up in water, basified to pH9-10 with 2N sodium hydroxide and extracted with ethyl acetate. The extracts were dried and evaporated to give the title compound (256 mg) as a pale yellow oil. Tic SiO2 (Dichloromethane/methanol/0.880 ammonia 75:8:1) Rf 0.53

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981572
Source datasetuspto-grants-1999_11
ORD IDord-8162816dff3743df98aae48742dfd4f9
Source noteuspto-grants-1999_11