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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22502Generated: October 25, 2026

2-Chloroethanol → 4-(2-Hydroxyethoxy)-3-methylmandelic acid

https://huagongshe.com/reaction/22502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-Hydroxy-3-methylmandelic acidHCID 23361405—
SolventWaterHCID 962—
Product4-(2-Hydroxyethoxy)-3-methylmandelic acidHCID 19930442—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 8.0 g (200 mmol) of sodium hydroxide in 15 ml of water is added dropwise over a period of one hour to a solution of 18.2 g (100 mmol) of 4-hydroxy-3-methylmandelic acid (Example 13), 4.0 g (100 mmol) of sodium hydroxide and 13.4 ml (200 mmol) of 2-chloroethanol in 60 ml water heated to 70° C. Another 6.7 ml (100 mmol) of 2-chloroethanol and 4.0 g (100 mmol) of sodium hydroxide in 10 ml of water are then added. After another 15 minutes, the reaction mixture is acidified with concentrated hydrochloric acid and extracted twice with ethyl acetate. The organic phases are washed with water, combined, dried over magnesium sulfate and concentrated on a vacuum rotary evaporator. This gives 23.0 g (about 100%) of 4-(2-hydroxyethoxy)-3-methylmandelic acid as a yellowish resin (compound (203), Table 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428162
Source datasetuspto-grants-1995_06
ORD IDord-5a8f3738e8b54083859973ad6d386fe0
Source noteuspto-grants-1995_06