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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262727Generated: November 4, 2026

Benzyl Bromide → HCID 15442177, compound

https://huagongshe.com/reaction/2262727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
ReactantHCID 15442175HCID 15442175—
SolventDimethylformamideHCID 6228—
ProductHCID 15442177HCID 15442177—

Reaction Steps

A mixture of tert-butyl 4-[(2-bromophenyl)carbamoyl]piperidine-1-carboxylate (8 mmol), benzylbromide (1.05 ml, 8.8 mmol) and Cs2CO3 (5.2 g, 16 mmol) in DMF (20 ml) is stirred at rt overnight. DMF is removed in vacuo and the residue is partitioned between H2O (40 ml) and EtOAc (40 ml). The layers are separated and the aqueous layer is extracted with EtOAc (20 ml). The combined extracts are washed with brine (20 ml), dried over Na2SO4 and evaporated. The residue is purified by flash column to give the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851474B2
Source datasetuspto-grants-2010_12
ORD IDord-1d677c01067c45c9b1cae1ce525951ef
Source noteuspto-grants-2010_12