HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252225Generated: October 25, 2026
Triethylamine → 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol
https://huagongshe.com/reaction/1252225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid | HCID 13334384 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol | HCID 20140800 | — |
Reaction Steps
To a mixture of 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid (14.0 g) and triethylamine (5.25 g) in tetrahydrofuran (280 ml), ethyl chloroformate (5.64 g) was added with ice-cooling and then stirred for 30 minutes. The resulting triethylamine hydrochloride was removed by filtration. To filtrate was added sodium borohydride (5 g) in water (90 mg) with ice-cooling, and the mixture was stirred for 1.5 hours. The reaction mixture was concentrated to a volume of 120 ml in vacuo and extracted with dichloromethane. The dichloromethane layer was washed with diluted hydrochloric acid and then water, dried over anhydrous sodium sulfate and evaporated in vacuo to give an oily residue which was then purified by silica gel chromatography to give 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742052 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-aeb5bb4dba7b42c5bfeaebee6c17486c |
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| Source note | uspto-grants-1988_05 |
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