Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30318Generated: October 26, 2026

Thionyl Chloride → 2-(Chloromethyl)-4-fluoro-1-methoxybenzene

https://huagongshe.com/reaction/30318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Fluoro-2-methoxyphenyl)methanolHCID 22014996—
SolventTolueneHCID 1140—
Product2-(Chloromethyl)-4-fluoro-1-methoxybenzeneHCID 30268661%

Reaction Steps

Neat (5-Fluoro-2-methoxy-phenyl)-methanol (19.587 g, 1 equiv.) is added to neat SOCl2 (42.2 mL, 4.6 equiv.) at −78° C. under a nitrogen atmosphere and the solution is then allowed to warm to room temperature and stirred until evolution of gas ceases. An equivalent volume of anhydrous toluene is added to the flask and the solution heated to 60° C. On cooling, the reaction solution is poured onto ice water. The toluene layer is separated and dried (MgSO4) and the solvent removed under reduced pressure. The crude material is sublimed (60-80° C./0.05 mBarr) to give the title compound as a white solid (13.40 g, 61%). MW 174.60; C8H8ClFO; 1H NMR (CDCl3): 3.87 (s, 3H), 4.60 (s, 2H), 6.79-7.20 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423037B2
Source datasetuspto-grants-2008_09
ORD IDord-022aabb333cd487794e3478b9e8ef063
Source noteuspto-grants-2008_09