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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080308Generated: October 31, 2026

3-Bromobenzaldehyde → 1,1-dimethylethyl (2S)-4-[(3-bromophenyl)methyl]-2-methyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/2080308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobenzaldehydeHCID 76583—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
SolventDichloromethaneHCID 6344—
Product1,1-dimethylethyl (2S)-4-[(3-bromophenyl)methyl]-2-methyl-1-piperazinecarboxylateHCID 5773671281.2%

Reaction Steps

A solution of 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate (100 mg, 0.5 mmol) in CH2Cl2 (5 mL) was mixed with 3-bromo benzaldehyde (0.06 mL, 0.5 mmol) and NaB(OAc)3H (0.16 g, 0.75 mmol). The resulting mixture was stirred for 12 hours, diluted with dichloromethane (30 mL) and washed with brine (50 mL). The organic layer was collected, dried over Na2SO4 and concentrated. Separation via a combiflash system then afforded the title compound (150 mg, 81%): LC/MS: m/z, 369 (M+H); 1HNMR (MeOD) δ 1.26 (3H, d), 1.47 (9H, s), 2.0 (1H, m), 2.1 (1H, m), 2.6 (1H, m), 2.8 (1H, m), 3.1 (1H, m), 3.3 (2H, s), 3.4 (1H, m), 3.5 (1H, m), 3.8 (1H, m), 4.2 (1H, m), 4.88 (1H, s), 7.25 (1H, m), 7.3 (1H, m), 7.4 (1H, m), 7.55 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932247B2
Source datasetuspto-grants-2011_04
ORD IDord-435a889393314cd4a1f294f3b451b068
Source noteuspto-grants-2011_04