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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585352Generated: October 31, 2026

Thionyl Chloride → 2-(Chloromethyl)anisole

https://huagongshe.com/reaction/1585352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Methoxybenzyl alcoholHCID 69154—
Reactant1,3-Benzodioxole, 5-(chloromethyl)-HCID 88713—
SolventDiethyl EtherHCID 3283—
Product2-(Chloromethyl)anisoleHCID 81495—

Reaction Conditions

Temperature0 °C

Reaction Steps

16.8 ml of thionyl chloride are added dropwise, over the space of approximately 30 min, to 10 ml of 2-methoxybenzyl alcohol (Fluka, Buchs, Switzerland) and 53.76 g of diisopropylaminomethylpolystyrene (polyhunig base, see Ex. 44a)) in 200 ml of abs. ether. After the mixture has been stirred at 0° C. for a further 1.5 h, it is filtered with suction and the filtrate is concentrated on a RE and under HV. The residue is purified by chromatography on silica gel (eluent: hexane/ethyl acetate, 6:1). TLC Rf (hexane:ethyl acetate=4:1)=0.5. 1H-NMR (200 MHz, CDCl3): 7.42-7.24 (m, 2H); 7.0-6.84 (m, 2H); 4.68 (s, 2H); 3.9 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935976
Source datasetuspto-grants-1999_08
ORD IDord-19df405b52794389b0d050e4bd7403dd
Source noteuspto-grants-1999_08