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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428905Generated: October 30, 2026

Hexylamine → 3-Hexyl-6-methyl-6-(3-nitrophenyl)-3-azabicyclo[3.1.0]hexan-2-one

https://huagongshe.com/reaction/428905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexylamineHCID 8102—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 3-(chloromethyl)-2-methyl-2-(3-nitrophenyl)cyclopropanecarboxylateHCID 22141336—
SolventWaterHCID 962—
Product3-Hexyl-6-methyl-6-(3-nitrophenyl)-3-azabicyclo[3.1.0]hexan-2-oneHCID 22141119—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl 3-(chloromethyl)-2-methyl-2-(3-nitrophenyl)cyclopropane carboxylate (Preparation 5, 20 g, 67.2 mmol) in hexylamine (36 ml, 270 mmol) was added sodium hydrogen carbonate (5.64 g, 67.2 mmol), and the mixture was heated at 100° C. for 16 h. The rmixture was cooled, diluted with water (80 ml) and extracted with dichloromethane (3×150 ml). The combined extracts were dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by silica column chromatography, eluting with a gradient of 2:1 to 1:2 hexane/ethyl acetate. Appropriate fractions were combined and concentrated in vacuo to give the title compound as a very pale yellow oil (14.2 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313312B1
Source datasetuspto-grants-2001_11
ORD IDord-2b23cb571cc542239f75b4a71f31a816
Source noteuspto-grants-2001_11