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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349389Generated: October 26, 2026

Benzene, 1-(chloromethyl)-2-fluoro- → [4-(2-Fluorobenzyloxy)-1-phenylcyclohexyl]dimethylamine

https://huagongshe.com/reaction/1349389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
Reactant4-Dimethylamino-4-phenylcyclohexanolHCID 11148709—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product[4-(2-Fluorobenzyloxy)-1-phenylcyclohexyl]dimethylamineHCID 1017202914.1%

Reaction Steps

2.75 g of 4-dimethylamino-4-phenylcyclohexanol were dissolved in 20 ml of dimethylformamide; 1.55 g of potassium tert.-butoxide were added and stirring was carried out for 45 minutes, before 2.0 g of 2-fluorobenzyl chloride were added dropwise in the course of 30 minutes. After stirring overnight, the mixture was added to 25 ml of ice-water and extracted repeatedly with ethyl acetate. The combined extracts were washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. The resulting crude product (3.41 g) was separated on silica gel with methanol/ethyl acetate (V:V=1:1). 580 mg of [4-(2-fluoro-benzyloxy)-1-phenylcyclohexyl]dimethylamine were obtained in the form of a white solid which, as described for Example 1, was converted into 370 mg of the corresponding hydrochloride using chlorotrimethylsilane and water in 2-butanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211694B2
Source datasetuspto-grants-2007_05
ORD IDord-a4e7e62514ce4b7ab369631794fd9ce5
Source noteuspto-grants-2007_05