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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33813Generated: October 24, 2026

Hydrochloric Acid → Methyl 2-chloro-3-[4-(2-hydroxyethyl)phenyl]propanoate

https://huagongshe.com/en/reaction/33813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl AcrylateHCID 7294—
Reactant4-Aminophenethyl alcoholHCID 66904—
ReactantSodium NitriteHCID 23668193—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductMethyl 2-chloro-3-[4-(2-hydroxyethyl)phenyl]propanoateHCID 8660080249%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(4-Aminophenyl)ethanol (11 g, 81 mmol) and 32 ml conc HCl was dissolved in acetone and cooled to 0° C. Sodium nitrite (5.6 g, 81 mmol) in 20 ml water was added dropwise. The temperature was kept under 0° C. After one hour, methyl acrylate (70 g, 808 mmol) and CuI (1.6 g, 8 mmol) were added (<0° C.). The reaction mixture was stirred at room temperature overnight. The solvent was evaporated and water was added. The water phase was extracted three times with EtOAc, the organic phases were pooled and washed with water, dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by flash chromatography using a 65:35 mixture of EtOAc and heptane as eluent. Further purification by preparative HPLC (using a gradient of CH3CN/5% CH3CN-waterphase containing 0.1M NH4OAc as eluent) gave 9.7 g product (yield 49%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429675B2
Source datasetuspto-grants-2008_09
ORD IDord-52e7e194b4d5420f8886f537fc483c0d
Source noteuspto-grants-2008_09