HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-Boc-1-fluoropent-4-EN-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | 1-Fluoropent-4-EN-2-amine hcl | HCID 20508329 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Boc-1-fluoropent-4-EN-2-amine | HCID 20508337 | 85% |
Reaction Steps
Tert-Butyloxycarbonyloxyimino-2-phenylacetonitrile (3.35 g, 13.6 mmoles) in dry tetrahydrofuran (40 ml) is slowly added with ice cooling to a stirred mixture of 1-fluoro-2-amino-4-pentene hydrochloride (1.9 g, 13.6 mmoles) and triethylamine (2.78 g, 27.2 mmoles) in tetrahydrofuran (30 ml). After standing overnight at room temperature, water is added, the tetrahydrofuran is removed under reduced pressure, and the residue is extracted twice with ether. After washing with 1 N sodium hydroxide, then with water until neutral, the organic layer is dried and stripped to give 1-fluoro-2-tert-butoxycarbonylamino-4-pentene (2.33 g, 85%) as an oil which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04375477 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-328d7ec2d5e34136ba793b896f94ba5d |
| Source note | uspto-grants-1983_03 |