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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362825Generated: October 30, 2026

Cyclopropylamine → HCID 10879452, compound

https://huagongshe.com/reaction/362825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantHCID 23293624HCID 23293624—
SolventDichloromethaneHCID 6344—
ProductHCID 10879452HCID 1087945276.4%

Reaction Steps

An ice cold solution of (E)-2-(4-choro-1-indanylidene)acetyl chloride (2.95 g, 0.013 mol ) in dichloromethane (30 mL) was treated with cyclopropylamine (1.48 g, 0.026 mol, Aldrich) and the mixture was stirred for 4 h. The mixture was concentrated in vacuo and the residue was taken up in a mixture of ethyl acetate and 5% aqueous sodium bicarbonate. The ethyl acetate phase was washed with 5% aqueous sodium bicarbonate, saturated aqueous NaCl and dried (Na2SO4). Filtration and concentration gave 3.5 g of crude oil product. Chromatography on Silca gel with ethyl acetate: hexanes (1:1) as eluent and trituration of the resulting solid with hexanes gave 2.46 g (76%) of (E)-2-(4-chloro-1-indanylidene)-N-cyclopropylacetamide as an off-white solid: m.p., 140°-142° C.; NMR (DMSO-d6): d 8.16, d, 1H, NH), 7.29-7.51 (m, 3H, Ar), 6.34 (t, 1H, =CH), 2.93-3.07, 3.18-3.31 (2m's, 4H 2XCH2), 2.72 (m, 1H, CH), 0.62-0.72, 0.39-0.47 (2m's, 4H, 2XCH2); steady-state nOe: irradiation at 6.34 d, observed 20.3% nOe at 7.46 d.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872118
Source datasetuspto-grants-1999_02
ORD IDord-e245599636d74ddf8dab512ecfcb24ab
Source noteuspto-grants-1999_02