Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486689Generated: October 30, 2026

N-bromobutanimide → 2-Amino-5-bromo-N,N-dimethyl-alpha-(3-methyl-2-thienyl)benzeneethanamine

https://huagongshe.com/reaction/486689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-amino-N,N-dimethyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 10061179—
SolventDimethylformamideHCID 6228—
Product2-Amino-5-bromo-N,N-dimethyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 2241448728.1%

Reaction Steps

To a solution of 6.0 g of 2-amino-N,N-dimethyl-α-(3-methyl-2-thienyl)benzeneethanamine in 30 ml of dimethylformamide, was added 5.32 g of N-bromosuccinimide in 30 ml of dimethylformamide, with stirring, and the mixture was stirred overnight at room temperature. The solution was concentrated, basified with 10% sodium hydroxide solution, and extracted with dichloromethane. The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by preparative HPLC (Water's Associates Prep LC/System 500a, silica gel, eluted with methanol, flow rate of 200 ml/min, Gow Mac model 80-800 UV detector). The appropriate fractions were collected and concentrated. The residue was dissolved in 100 ml of diethylether and filtered. The filtrate was concentrated. The residue was triturated in hexane to give 2.2 g of product, mp 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292760
Source datasetuspto-grants-1994_03
ORD IDord-84683e8ed9dc4041a38f3c020ad301b7
Source noteuspto-grants-1994_03