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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058657Generated: October 31, 2026

Benzene, 1-(chloromethyl)-2-fluoro- → N-(2-fluorophenylmethyl)-3-hydroxy-N-methyl-3-phenylpropylamine

https://huagongshe.com/reaction/2058657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant3-Methylamino-1-phenylpropanolHCID 2733989—
SolventAcetonitrileHCID 6342—
ProductN-(2-fluorophenylmethyl)-3-hydroxy-N-methyl-3-phenylpropylamineHCID 1295184375.1%

Reaction Steps

A mixture of 3-hydroxy-N-methyl-3-phenylpropylamine (8.3 g, 50 mM), 2,2,6,6-tetramethylpiperidine (8.4 ml, 50 mM), o-fluorobenzyl chloride (7.25 g, 50 mM) and acetonitrile (100 ml) was stirred for 24 hours at ambient temperature. The resulting precipitate was removed by filtration, the precipitate washed with acetonitrile and the combined filtrate and washings evaporated under reduced pressure. The residue was partitioned between 2 N hydrochloric acid (100 ml) and ether (100 ml), the aqueous layer basified and extracted with ether (2×100 ml). The ether extract was dried and the solvent removed under reduced pressure to yield an oil (10.3 g). Distillation gave the title compound b.p. 160°-2° C./0.6 mbar. Found: C, 74.4; H, 7.3; N, 5.4%; C17H20FNO requires: C, 74.7; H, 7.4; N, 5.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04318909
Source datasetuspto-grants-1982_03
ORD IDord-189f0688608445a68a3bc023e40c4049
Source noteuspto-grants-1982_03