Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419820Generated: November 4, 2026

Sodium Hydroxide → N-[4-Chloro-3-(2-dimethylaminoethoxy)phenyl]aminoacetaldehyde dimethyl acetal

https://huagongshe.com/reaction/1419820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantAcetaldehyde, 2,2-dimethoxy-HCID 162650—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Chloro-3-(2-dimethylamino-ethoxy)anilineHCID 12135420—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-[4-Chloro-3-(2-dimethylaminoethoxy)phenyl]aminoacetaldehyde dimethyl acetalHCID 5702712987%

Reaction Steps

To a suspension of 4-chloro-3-(2-dimethylaminoethoxy)aniline (1.22 g, 0.006 mol) in MeOH (30 ml) containing dimethoxyethanal in MTBE (1.76 g, 0.17 mol) and glacial acetic acid (1.71 g) was added sodium cyanoborohydride (1.78 g, 0.03 mol ) portionwise at 0° C. The reaction was left to stir at room temperature for 1 hour, and then 10% aq. NaOH was added and the mixture was extracted with CH2Cl2. The combined organic layers were dried (Na2SO4), and concentrated in vacuo to give a brown oil. Purification by FCC, eluting with CH2Cl2 gave the title compound (1.49 g, 87%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889022
Source datasetuspto-grants-1999_03
ORD IDord-1d2e122cd4584aa393c74679c098e8fe
Source noteuspto-grants-1999_03