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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443099Generated: October 30, 2026

2-Methoxyphenylacetic acid → 2-(5-Chloro-2-methoxyphenyl)acetic acid

https://huagongshe.com/reaction/443099

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxyphenylacetic acidHCID 7134—
ReactantTetrahydrofuranHCID 8028—
ReactantSulfuryl chlorideHCID 24648—
SolventWaterHCID 962—
Product2-(5-Chloro-2-methoxyphenyl)acetic acidHCID 150404795%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A flame dried three-necked 3-L round-bottomed flask, equipped with a septa, stirring bar, argon inlet, thermocouple and addition funnel capped with a septa, was vacuum/argon purged. The flask was charged with commercially available 2-methoxy phenylacetic acid (300 g, 1.81 mol) and anhydrous THF (2 L). The mixture was cooled to approximately -15° C. and stirred until the solution became homogeneous. Neat sulfuryl chloride (205 mL, 2.55 mol) was added dropwise via an additional funnel while stirring over an hour. The internal temperature was maintained below -5° C. (ranging between -15° and -5° C.). Immediately after the complete addition of sulfuryl chloride, HPLC analysis showed the reaction was complete. The reaction mixture was poured into cold water (16 L) with vigorous stirring. The resultant slurry was stirred for 3 hours and the white precipitate was collected by filtration, washed with water (2 L), air dried for about 24 h, and vacuum dried to afford 345.3 g (95% yield, 97% by HPLC) of the title compound as an off-white solid that was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05892106
Source datasetuspto-grants-1999_04
ORD IDord-542764c8b8e64036ae4c5483b630a2fa
Source noteuspto-grants-1999_04