Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397836Generated: October 30, 2026

Ethyl Acetate → [2-(2,4-dichlorophenoxy)phenyl]methanol

https://huagongshe.com/reaction/397836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BisulfateHCID 516919—
Reactant2-(2,4-dichlorophenoxy)benzaldehydeHCID 2763427—
ReactantSodium borohydrideHCID 4311764—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
Product[2-(2,4-dichlorophenoxy)phenyl]methanolHCID 276366872.7%

Reaction Steps

Sodium borohydride (119 mg, 3.15 mmol) was added to a solution of 2-(2,4-dichlorophenoxy)benzaldehyde (600 mg, 2.25 mmol) in isopropanol (10 ml) and DCM (20 ml). The reaction mixture was stirred for 2 hours at room temperature. A 10% aqueous solution of sodium hydrogensulphate (200 ml) was added dropwise. Ethyl acetate (300 ml) was added successively. The phases were separated. The aqueous phase was extracted with ethyl acetate (100 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane 1:3 as eluent, to give 440 mg of 1-[2-(2,4-dichlorophenoxy)phenyl]methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610721B2
Source datasetuspto-grants-2003_08
ORD IDord-cf8927e643d74c7bb859e972a021e2c0
Source noteuspto-grants-2003_08