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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424808Generated: October 30, 2026

2-Butoxy-4-formyl-benzoic Acid Methyl Ester → 2-Butoxy-4-({[4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-benzoic Acid Methyl Ester

https://huagongshe.com/reaction/424808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butoxy-4-formyl-benzoic Acid Methyl EsterHCID 57443319—
Reactant4-[(tert-butyldimethylsilyl)oxy]-N,2-dimethylanilineHCID 66704120—
Reactant4-({[4-(Tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-2-methyl-benzoic acid methyl esterHCID 66704169—
Product2-Butoxy-4-({[4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-benzoic Acid Methyl EsterHCID 66704181—

Reaction Steps

The title compound is prepared by reductive amination of [4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amine with 2-butoxy-4-formyl-benzoic acid methyl ester, essentially as described in the synthesis of 4-({[4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-2-methyl-benzoic acid methyl ester using the appropriate starting material. The title compound is obtained as syrup after workup. LC-ES/MS m/e 472.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106077B2
Source datasetuspto-grants-2012_01
ORD IDord-0d21f20779364c87894f4c8590f3927a
Source noteuspto-grants-2012_01