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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671539Generated: October 29, 2026

Ammonium Chloride → Cholest-5-en-3-yl 2-(4-aminobenzyl)-3-(4-aminophenyl)propanoate

https://huagongshe.com/reaction/1671539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantCholest-5-en-3-yl 2-(4-nitrobenzyl)-3-(4-nitrophenyl)propanoateHCID 86602370—
CatalystZincHCID 23994—
SolventMethanol--water (1/1)HCID 22242641—
ProductCholest-5-en-3-yl 2-(4-aminobenzyl)-3-(4-aminophenyl)propanoateHCID 6734870569.3%

Reaction Steps

2.62 g (3.75 mmol) Cholest-5-en-3-yl 2-(4-nitrobenzyl)-3-(4-nitrophenyl)-propanoate and 0.79 g (14.77 mmol) ammonium chloride were suspended in 90 ml of a mixture consisting of methanol:water 9:1. 4.90 g (74.96 mmol) zinc powder was then added in 10 minutes. The reaction mixture was then allowed to react at 45° C. for 6 hours and partitioned between dichloromethane and water; the organic phase was washed repeatedly with water, dried over sodium sulfate, filtered and concentrated by rotary evaporation. First chromatography of the residue on 50 g silica gel using toluene:ethyl acetate 1:1 as eluant and second chromatography on 50 g silica gel using tert.butyl methylether as eluant yielded 1.66 g Cholest-5-en-3-yl 2-(4-aminobenzyl)-3-(4-aminophenyl)propanoate as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994273B2
Source datasetuspto-grants-2011_08
ORD IDord-8a7fa7e663d4459fab0d3c813c9f0cda
Source noteuspto-grants-2011_08