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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant(2R)-2-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6995000—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product((r)-1-Phenylcarbamoyl-butyl)-carbamic acid tert-butyl esterHCID 68777029—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790747B2
Source datasetuspto-grants-2010_09
ORD IDord-cf77be83f5d24430af3838ebdf0ec806
Source noteuspto-grants-2010_09