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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049647Generated: November 2, 2026

Thionyl Chloride → 1-(Chloromethyl)-2-(4-fluorophenoxy)benzene

https://huagongshe.com/reaction/2049647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 3700253HCID 3700253—
SolventBenzeneHCID 241—
Product1-(Chloromethyl)-2-(4-fluorophenoxy)benzeneHCID 20343827—

Reaction Steps

8.5 g of thionyl chloride are added dropwise over a 10 minutes span to a stirring mixture of 13.0 g of 2-(4-fluorophenoxy)benzyl alcohol in 80 ml of benzene at ambient temperature. After total addition, the reaction mixture is stirred for 16 hours before being carefully poured onto 350 ml of crushed ice containing 8 ml of sodium bicarbonate. The mixture is stirred until the ice melts. The layers separate and the benzene layer is successively washed twice with 40 ml portions of a half saturated sodium bicarbonate solution, washed twice with 40 ml portions of water, washed once with a 25 ml portion of a saturated sodium chloride solution, dried and rotary evaporated to provide a clear liquid. The liquid is distilled at 106°-109° C. and 0.16 mm to provide a clear colorless liquid of 2-(4-fluorophenoxy)benzyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198418
Source datasetuspto-grants-1980_04
ORD IDord-c4d013f87d784d7dba26ac0afe834a9a
Source noteuspto-grants-1980_04