HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-(tert-Butoxycarbonylaminomethyl)-3-phenylisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-hydroxybenzenecarboximidoyl chloride | HCID 2756315 | — |
| Reactant | tert-butyl N-(prop-2-yn-1-yl)carbamate | HCID 11073648 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(tert-Butoxycarbonylaminomethyl)-3-phenylisoxazole | HCID 67283792 | 54% |
Reaction Steps
A solution of α-chlorobenzaldehyde oxime (Method 22; 1 g, 6.4 mmol) in THF (13 ml) was added dropwise to a solution of N-tert-butoxycarbonyl-propargylamine (0.5 g, 3.2 mmol) and triethylamine (0.9 ml, 6.4 mmol) in THF (25 ml) cooled with an ice bath. The mixture was allowed to warm to ambient temperature and stirred for 2 days. The volatiles were removed by evaporation and the residue dissolved in DCM. The solution was washed with water and brine, dried (MgSO4) and the solvent removed by evaporation. The residue was triturated with isohexane/ether (9:1) and collected by filtration to give the title compound (473 mg, 54%). NMR (CDCl3) 1.45 (s, 9H), 4.45 (d, 2H), 5.10 (bs, 1H), 6.5 (s, 1H), 7.42 (m, 3H), 7.8 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07521453B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-b58b1f272343400a9b2fbe052cc1e33a |
| Source note | uspto-grants-2009_04 |