HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711194Generated: November 4, 2026
Aniline → ((r)-1-Phenylcarbamoyl-butyl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1711194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (2R)-2-(((tert-butoxy)carbonyl)amino)pentanoic acid | HCID 6995000 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ((r)-1-Phenylcarbamoyl-butyl)-carbamic acid tert-butyl ester | HCID 68777029 | — |
Reaction Steps
To a 0° C. solution of the crude carboxylic acid (652 mg, 3.00 mmol) and NMM (0.50 ml, 4.5 mmol) in THF (12 ml) was added isobutyl chloroformate (0.45 ml, 3.5 mmol) and the resulting mixture was stirred at 0° C. for 5 minutes. A solution of aniline (0.45 ml, 4.9 mmol) in THF (3 ml) was then added dropwise. The reaction was warmed to room temperature and stirred for 66 hours. The reaction was diluted with 1M HCl (30 ml) and was extracted with Et2O (25 ml×3). The organic solution was washed with brine (50 ml), was dried (Na2SO4), filtered and concentrated under reduced pressure, giving crude ((R)-1-phenylcarbamoyl-butyl)-carbamic acid tert-butyl ester as an oily, light yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07790747B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-cf77be83f5d24430af3838ebdf0ec806 |
|---|
| Source note | uspto-grants-2010_09 |
|---|