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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382202Generated: October 31, 2026

Triethylamine → (R)-Tert-butyl 4-benzyl-2-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/2382202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant(R)-1-Benzyl-3-methylpiperazineHCID 6923226—
SolventDichloromethaneHCID 6344—
Product(R)-Tert-butyl 4-benzyl-2-methylpiperazine-1-carboxylateHCID 1008563485.1%

Reaction Steps

To a solution of (R)-1-benzyl-3-methylpiperazine (10 g, 52.6 mmol) in dichloromethane (30 mL) at room temperature was added triethylamine (10.6 g, 106 mmol) and the reaction mixture was stirred for 1 h. To the reaction mixture was added (BOC)2O (13.7 g, 62.8 mmol) and the contents were stirred for further 4 h. The reaction mixture was quenched in water and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the crude product. The crude product was purified by silica gel (100-200 mesh) column chromatography eluting with 10% ethyl acetate in n-hexanes to afford 13.0 g of (R)-tert-butyl 4-benzyl-2-methylpiperazine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258306B2
Source datasetuspto-grants-2012_09
ORD IDord-cda46e477d794b1b897e262014fc7021
Source noteuspto-grants-2012_09