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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857158Generated: October 31, 2026

Benzaldehyde → Methyl[3,5-dichloro-4-(4-benzylaminophenoxy)phenyl]acetate

https://huagongshe.com/reaction/857158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 21867227HCID 21867227—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductMethyl[3,5-dichloro-4-(4-benzylaminophenoxy)phenyl]acetateHCID 2186725588.1%

Reaction Steps

A stirred mixture consisting of methyl[3,5-dichloro-4-(4-aminophenoxy)phenyl]acetate (0.32 g), benzaldehyde (0.20 g), sodium cyanoborohydride (0.03 g), methanol (15 mL) and one drop of acetic acid was stirred at room temperature for 5 days. The reaction mixture was concentrated and the residue partionated between ethyl acetate and sodium hydrogen-carbonate (saturated aqueous solution). The aqueous phase was further extracted with ethyl acetate. The collected organic phases were purified on column (silica gel, n-heptane/ethyl acetate, 9:1) to give 0.36 g of methyl[3,5-dichloro-4-(4-benzylaminophenoxy)phenyl]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144909B2
Source datasetuspto-grants-2006_12
ORD IDord-20959f241126469db4f1c93a84be82a3
Source noteuspto-grants-2006_12