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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852757Generated: November 4, 2026

Benzylamine → 6-Benzyl-6-azabicyclo[3.1.0]hexan-2-one

https://huagongshe.com/reaction/1852757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant2-Cyclopenten-1-one, 2-bromo-HCID 3014641—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product6-Benzyl-6-azabicyclo[3.1.0]hexan-2-oneHCID 12119765—

Reaction Steps

To a stirred solution of 2-bromocyclopent-2-enone (1.00 g, 6.21 mmol) in H2O (25 mL), tetrabutylammonium bromide (400 mg, 1.24 mmol) and benzyl amine (790 mg, 7.45 mmol) were added at room temperature. The reaction mixture was stirred for 24 hours and then extracted with EtOAc (100 mL). The organic layer was separated, washed with brine, and dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification of the residue on a silica gel column with 0 to 30% EtOAc/Hexanes afforded 6-benzyl-6-azabicyclo[3.1.0]hexan-2-one. MS ESI calc'd. for C12H13NO [M+H]+ 188. found 188.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962611B2
Source datasetuspto-grants-2015_02
ORD IDord-d8278f8231a74defaeaaeb7056934d18
Source noteuspto-grants-2015_02