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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369112Generated: October 30, 2026

Hydrochloric Acid → [4-(3,4-Dichloro-benzyloxy)-phenyl]-hydroxy-acetic acid

https://huagongshe.com/reaction/2369112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantEthyl AcetateHCID 8857—
Reactant3,4-Dichlorobenzyl 2-(4-((3,4-dichlorobenzyl)oxy)phenyl)-2-hydroxyacetateHCID 66922590—
SolventMeOH tetrahydrofuranHCID 21899815—
Product[4-(3,4-Dichloro-benzyloxy)-phenyl]-hydroxy-acetic acidHCID 66923034—

Reaction Steps

2-[4-(3,4-Dichloro-benzyloxy)-phenyl]-2-hydroxy-acetic acid 3,4-dichloro-benzyl ester (9.4 g,) was dissolved in 120 mL of THF-methanol (4:1) and 2N lithium hydroxide solution (39 mL) added. The resulting reaction mixture was stirred at room temperature 16 h. The mixture was poured onto 1N HCl and EtOAc and the organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residual oil was taken up in minimal DCM and hexanes added to give a solid. The solid was filtered and washed with hexanes to afford the desired product [4-(3,4-dichloro-benzyloxy)-phenyl]-hydroxy-acetic acid in pure form (6.1 g). 1H NMR (400 MHz, DMSO d6): 7.69 (d, 1H), 7.63 (d, 1H), 7.41 (m, 1H), 7.31 (m, 2H), 6.96 (m, 2H), 5.10 (s, 2H), 4.94 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703766B2
Source datasetuspto-grants-2014_04
ORD IDord-b045e81650684864a4c2bd25ac5e7888
Source noteuspto-grants-2014_04