HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 4-Methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid p-methoxybenzyl ester | HCID 53971933 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid | HCID 13334384 | — |
Reaction Steps
A mixture of 4-methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid p-methoxybenzyl ester (25 g), anisole (25 g) and trifluoroacetic acid (125 ml) was stirred for 15 minutes at room temperature. Evaporation of trifluoroacetic acid gave an oily residue which was then dissolved in diethyl ether. The ether solution was extracted with aqueous sodium carbonate. The aqueous layer was washed with diether ether, acidified with dilute hydrochloric acid and extracted with benzene. The benzene extract was washed with water, dried over anhydrous sodium sulfate and evaporated to give 4-methyl-4-p-nitrobenzyloxycarbonylaminovaleric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742052 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-ee09b96d6f97420b9c4ef0a3e6050de5 |
| Source note | uspto-grants-1988_05 |