HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004570Generated: October 26, 2026
Bromoacetyl bromide → (+,-)-Bromoacetyl-2-(3,4-dichlorophenyl)-4-(3,5-dimethylbenzoyl)piperazine
https://huagongshe.com/reaction/1004570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazine | HCID 10292159 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+,-)-Bromoacetyl-2-(3,4-dichlorophenyl)-4-(3,5-dimethylbenzoyl)piperazine | HCID 10277726 | 47.3% |
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]+35Cl,79Br482.9, 484.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051575 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-7a80d2f7296b4f09961ae1bb342cafa7 |
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| Source note | uspto-grants-2000_04 |
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