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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721344Generated: October 31, 2026

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

https://huagongshe.com/reaction/1721344

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 numberUS05510346
Source datasetuspto-grants-1996_04
ORD IDord-1db40201c3304180916c7b6f903cd427
Source noteuspto-grants-1996_04