HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391042Generated: October 30, 2026
Triethylamine → (1R)-1-Phenylethyl N-(5-(4-bromophenyl)-3-methyl-4-isoxazolyl)carbamate
https://huagongshe.com/reaction/2391042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 1-Phenylethanol, (R)- | HCID 637516 | — |
| Reactant | 5-(4-Bromophenyl)-3-methyl-1,2-oxazole-4-carboxylic acid | HCID 56604559 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (1R)-1-Phenylethyl N-(5-(4-bromophenyl)-3-methyl-4-isoxazolyl)carbamate | HCID 66660383 | — |
Reaction Steps
5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carboxylic acid (2.0 g, 7.09 mmol) and triethylamine (0.99 mL, 7.09 mmol) were dissolved in toluene (50 mL). Diphenylphosphoryl azide (1.5 mL, 7.09 mmol) was added, followed by (R)-(+)-1-phenylethyl alcohol (0.865 g, 7.09 mmol; commercially available or prepared using procedures described herein or in the literature: e.g. E. J. Corey et al. J. Am. Chem. 1987, 109, 5551-5553), and the reaction was stirred at 80° C. for 4 hours. The mixture was concentrated, and the residue was purified by silica gel chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273780B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-16bf6d0ce4dd44288739f885dc35f80c |
|---|
| Source note | uspto-grants-2012_09 |
|---|