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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530517Generated: November 1, 2026

Chloroacetic Acid → (2-Phenylethoxy)acetic acid

https://huagongshe.com/reaction/530517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantHydrochloric AcidHCID 313—
Reactant2-PhenylethanolHCID 6054—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(2-Phenylethoxy)acetic acidHCID 1320892275.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred mixture of phenethyl alcohol (1.0 g, 8.18 mmol) in DMSO (16 mL) under nitrogen flow, NaH (0.39 g, 16.37 mmol) was added in one portion and the mixture was stirred at 60° C. for 10 min. Following the addition of chloroacetic acid (0.77 g, 8.18 mmol), the reaction mixture was heated at 80° C. for 3 h. The cooled mixture was then poured into H2O and the aqueous phase acidified to pH 1.0 with a 2.0 N HCl solution. The aqueous phase was then extracted with EtOAc (3×20 mL), and the combined organic phase washed with brine and dried over Na2SO4 to afford the title compound (1.11 g, 75%), which was used in the following step without further purification. 1H NMR (DMSO-d6): δ 2.83 (t, J=7.0 Hz, 2H), 3.67 (t, J=7.0 Hz, 2H), 4.00 (s, 2H), 7.15-7.32 (m, 5H), 12.64 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353075B2
Source datasetuspto-grants-2016_05
ORD IDord-01c5c7980a224801904c49fc7201d7e3
Source noteuspto-grants-2016_05