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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086054Generated: October 25, 2026

Triphenylphosphine → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(3-methoxy-butoxy)-benzamide

https://huagongshe.com/reaction/1086054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Methoxy-1-butanolHCID 17291—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanto-Desmethyl metoclopramideHCID 9817332—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(3-methoxy-butoxy)-benzamideHCID 992937652.4%

Reaction Steps

A stirred solution of 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (1.715 g, 6 mmoles; prepared according to Preparation 1B), triphenylphosphine (1.58 g, 6 mmoles), 3-methoxy-1-butanol (0.62 g, 6 mmoles) in dry tetrahydrofuran (50 ml) was treated dropwise with diethyl azodicarboxylate (1.1 g of 95% purity material, 6 mmoles). The solution was left to stir overnight. After evaporation of the solvent the residue was dissolved in methylene chloride. The solution was washed with 0.4N NaOH, water, dried and the solvent evaporated. The residue was chromatographed over deactivated silica using methylene chloride (100), methanol (2.5), ammonium hydroxide (0.5) solvent system. The appropriate fractions were combined and the solvent evaporated. The residue (1.7 g) was crystallized from toluene to yield 1.17 g (52%) of the title compound, m.p. 76°-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011992
Source datasetuspto-grants-1991_04
ORD IDord-1b7719b6b01648a6ac7203494b20496f
Source noteuspto-grants-1991_04