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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Cholest-5-en-3-yl 2-(4-nitrobenzyl)-3-(4-nitrophenyl)propanoate | HCID 86602370 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | Cholest-5-en-3-yl 2-(4-aminobenzyl)-3-(4-aminophenyl)propanoate | HCID 67348705 | 69.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994273B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8a7fa7e663d4459fab0d3c813c9f0cda |
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| Source note | uspto-grants-2011_08 |
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