HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 70050348, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | Methyl 4-aminobenzoate | HCID 12082 | — |
| Reactant | benzyl (2S)-2-amino-3-methylbutanoate | HCID 6950584 | — |
| Product | HCID 70050348 | HCID 70050348 | — |
Reaction Steps
To a solution of methyl p-aminobenzoate (0.4 g) in tetrahydrofuran (10 ml) was added trichloromethylchloroformate (0.31 g) and the mixture was allowed to stand overnight at room temperature. L-Valine benzyl ester (0.54 g) was added to the solution and the pH of the mixture was neutralized with triethylamine. After being stirred for 30 minutes at room temperature, the mixture was concentrated under reduced pressure and the residue was extracted with ethyl acetate (10 ml). The extract was washed with 1N-hydrochloric acid (10 ml) and aqueous sodium bicarbonate (10 ml) and concentrated to dryness to give 4-(methoxycarbonyl)phenylaminocarbonyl-L-valine benzyl ester (1.17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05430025 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-1760c07e0d5546cf8f11bd102b954cdf |
| Source note | uspto-grants-1995_07 |