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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750501Generated: October 26, 2026

Water → 1-Methyl-6-(4-methylbenzenesulfonyl)-6-azabicyclo[3.1.0]hexane

https://huagongshe.com/reaction/1750501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylcyclopenteneHCID 12746—
ReactantChloramine-THCID 3641960—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-6-(4-methylbenzenesulfonyl)-6-azabicyclo[3.1.0]hexaneHCID 118024580—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-methylcyclopent-1-ene (CAS number 693-89-0; 50.0 g, 609.75 mmol) iii and sodium chloro(4-methylbenzenesulfonyl)azanide (CAS number 127-65-1; 192 g, 680.85 mmol) in THF (2500 ml) was added trimethylphenylammonium tribromide (13.3 g, 61.57 mmol). The reaction was stirred vigorously at 25° C. for 12 hours. The reaction mixture was poured into water (1500 ml) and the organics were extracted with ethyl acetate (3×1000 ml). The combined organics were washed with water (500 ml), brine (500 ml), dried over sodium sulfate and concentrated in vacuo. This was then purified by column chromatography (silica, 0-2.5% ethyl acetate/n-hexane) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156829B2
Source datasetuspto-grants-2015_10
ORD IDord-3662870c197c4417a45b083481a04d69
Source noteuspto-grants-2015_10