Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717640Generated: October 30, 2026

Ethyl 3-(5-(oct-1-ynyl)indoline-1-carboxamido)propanoate → HCID 66614892, compound

https://huagongshe.com/reaction/717640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(5-(oct-1-ynyl)indoline-1-carboxamido)propanoateHCID 66615094—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 66614892HCID 6661489290%

Reaction Steps

A mixture of the product of Step C (0.1 g; 0.27 mmol) and 10% Pd/C (0.1 g) in EtOH (15 ml) was stirred at room temperature for 1 h under H2 (balloon). The catalyst was removed by filtration through the Celite pad, washed with CH2Cl2 (2×10 ml) and combined filtrates were evaporated to dryness under reduced pressure to give a title compound (0.09 g; 90%), as colourless solid. 1H-NMR (CDCl3) 7.71 (d, 1H, J=8.8 Hz); 6.94 (d, 1H, J=8.8 Hz); 6.93 (s, 1H); 5.29 (m, 1H); 4.14 (q, 2H, J=7 Hz); 3.82 (t, 2H, J=8.8 Hz); 3.57 (q, 2H, J=5.9 Hz); 3.11 (t, 2H, J=8.6 Hz); 2.59 (t, 2H, J=5.7 Hz); 2.51 (t, 2H, J=7.7 Hz); 1.57 (m, 2H); 1.26 (m, 13H); 0.86 (t, 3H, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193716B2
Source datasetuspto-grants-2015_11
ORD IDord-5afdf111d5304ae29cba8b3a9679c037
Source noteuspto-grants-2015_11