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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480684Generated: October 29, 2026

Acetic Acid → Ethyl 2-[3-[N-(4-Chlorobenzyl)aminomethyl]phenoxy]-2-methylpropionate

https://huagongshe.com/reaction/480684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzylamineHCID 66036—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 2-(3-formylphenoxy)-2-methylpropanoateHCID 18766496—
Solvent1,2-DichloroethaneHCID 11—
SolventChloroformHCID 6212—
ProductEthyl 2-[3-[N-(4-Chlorobenzyl)aminomethyl]phenoxy]-2-methylpropionateHCID 18766446—

Reaction Steps

Ethyl 2-(3-formylphenoxy)-2-methylpropionate (25 g, 105.8 mmol) was dissolved in 1,2-dichloroethane (300 mL). Subsequently, 4-chlorobenzylamine (15.44 mL, 127.0 mmol) and acetic acid (7.26 mL, 127.0 mmol) were added thereto, and the resultant mixture was stirred for 20 minutes at 0° C. Subsequently, sodium (triacetoxy)borohydride [NaBH(OAc)3 (26.91 g, 127.0 mmol)] was added thereto, and the mixture was stirred for five hours at room temperature. After completion of reaction, chloroform was added. Washing was performed sequentially with aqueous saturated sodium bicarbonate, water, and saturated brine, followed by drying over magnesium sulfate. The reaction mixture was subjected to filtration, concentration under reduced pressure, and purification by silica gel column chromatography (chloroform/methanol=10/1), whereby a yellow oil was obtained (35.27 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653334B1
Source datasetuspto-grants-2003_11
ORD IDord-391fd4c2304d4c708005fedc0f65078d
Source noteuspto-grants-2003_11