HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597676Generated: October 27, 2026
L-Phenylalanine → (2S)-2-[(4-methoxyphenyl)methoxycarbonylamino]-3-phenylpropanoic acid
https://huagongshe.com/reaction/597676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile | HCID 3916227 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2S)-2-[(4-methoxyphenyl)methoxycarbonylamino]-3-phenylpropanoic acid | HCID 11823666 | 64.7% |
Reaction Steps
2-(4-Methoxybenzyl)oxycarbonyloxyimino-2-phenylacetonitrile (1.55 g.) was added to a solution of L-phenylalanine (826 mg.) and triethylamine (0.75 ml.) in a mixture of methanol (10 ml.), dioxane (1.5 ml.) and water (7.5 ml.) at room temperature the resulting mixture was stirred for 2 hours at room temperature. The reaction mixture was concentrated and benzene and a sodium bicarbonate aqueous solution were added to the residue. After shaking the resultant mixture, the aqueous layer was separated from the mixture, washed with ether, acidified with hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried and concentrated. N-Hexane was added to the residue, and the precipitated crystals were collected by filtration and dried to give N-(4-methoxybenzyl)oxycarbonyl-L-phenylalanine (1.064 g.), mp 87° to 88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04014915 |
|---|
| Source dataset | uspto-grants-1977_03 |
|---|
| ORD ID | ord-dfb3965047144e62a4ddb4cd19cc9dee |
|---|
| Source note | uspto-grants-1977_03 |
|---|