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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362539Generated: October 26, 2026

Bromoacetyl bromide → (+,-)-Bromoacetyl-2-(3,4-dichlorophenyl)-4-(3,5-dimethylbenzoyl)piperazine

https://huagongshe.com/reaction/362539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantDiisopropylethylamineHCID 81531—
Reactant(+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazineHCID 10292159—
SolventDichloromethaneHCID 6344—
Product(+,-)-Bromoacetyl-2-(3,4-dichlorophenyl)-4-(3,5-dimethylbenzoyl)piperazineHCID 1027772647.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled solution of (+,-)-[3,5-dimethylbenzoyl]-3-(3,4-dichlorophenyl)piperazine (11.5 g, 31.65 mmol) in CH2Cl2 (200 mL) at 0° C. was added Hunig's base (4.5 g, 35 mmol) and bromoacetyl bromide (6.4 g, 31.65 mmol). The solution was stirred at 0° C. overnight under N2. After completion the reaction was diluted with CH2Cl2 (400 mL) and washed with brine (300 mL, 2×), dried over MgSO4, filtered and concentrated. The crude material was purified by flash grade silica gel chromatography, eluting with 2% [NH4OH/MeOH (1:9)]/98% CH2Cl2 to give the title compound as a light yellow solid (7.1 g, 47.3%), m.p. 77°-79° C., FAB MS [M+1]+ 35 Cl, 79Br 482.9, 484.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869488
Source datasetuspto-grants-1999_02
ORD IDord-98185fac8ad14c8fb692e9e31d8a7ca0
Source noteuspto-grants-1999_02