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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987576Generated: October 30, 2026

Dichloromethane → 8-(2-Chloroethyl)-3-(2-naphthyl)-8-azabicyclo[3.2.1]oct-2-ene

https://huagongshe.com/reaction/987576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-[3-(2-Naphthyl)-8-azabicyclo[3.2.1]oct-2-en-8-yl]ethanolHCID 18009172—
SolventWaterHCID 962—
Product8-(2-Chloroethyl)-3-(2-naphthyl)-8-azabicyclo[3.2.1]oct-2-eneHCID 1800918150%

Reaction Steps

2-[3-(2-Naphthyl)-8-azabicyclo[3.2.1]oct-2-en-8-yl]ethanol (0.95 g, 3.40 mmol), 0.42 g (3.70 mmol) MsCl, 0.71 mL (515 mg, 5.10 mmol) Et3N and 20 mL CH2Cl2 are stirred at 23 C in for 12 h. The reaction mixture is poured into 200 mL of H2O and extracted with 3×50 mL CH2Cl2. The combined organics are washed with H2O (3×100 mL,) brine (1×100 mL), dried over MgSO4, filtered, and the volatiles are evaporated. Flash chromatography on SiO2 gel, eluting with EtOAc/MeOH (20/1 to 10/1), gives 0.50 g (1.68 mmol, a 50% yield) of the title compound as a tan solid. mp: 122-123° C.; MS (ES) m/z 298 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632824B2
Source datasetuspto-grants-2003_10
ORD IDord-3c02c04b044a409c8986b1f6f8aad795
Source noteuspto-grants-2003_10