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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969422Generated: October 31, 2026

Aniline → Ethyl 1-(phenylaminocarbonyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1969422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1-(Ethoxycarbonyl)cyclopropanecarboxylic acidHCID 11789472—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-(phenylaminocarbonyl)cyclopropanecarboxylateHCID 1415021889%

Reaction Steps

To a solution of 1-(ethoxycarbonyl)cyclopropane carboxylic acid (7.4 g, 46.84 mmol) in dry CH2Cl2 (70 mL) was added HATU (35.62 g, 93.67 mmol) at 0° C. After stirring for 10 minutes, a solution of the aniline (8.71 g, 93.67 mmol) and Et3N (9.48 g, 93.67 mmol) in dry CH2Cl2 (30 mL) was then added and the reaction mixture was continued to stir at 40° C. for 24 hrs. The reaction mixture was quenched with water (30 mL) and extracted with CH2Cl2 (100 mL×3). The combined organic phases were dried over anhydrous Na2SO4, filtered and the filtrate was concentrated in vacuo. The residue was chromatographed with a silica gel column (1:5 (v/v) EtOAc/n-hexane) to afford the title compound as a pale yellow solid (9.7 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426585B2
Source datasetuspto-grants-2013_04
ORD IDord-f96bb16697e94af587a9c9bcb8ef1bd5
Source noteuspto-grants-2013_04