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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047771Generated: November 1, 2026

2-[2-(-1-Ethyl-but-1-enyl)-3-methyl-benzoylamino]-indan-2-carboxylic acid → 2-[2-(1-Ethyl-butyl)-3-methyl-benzoylamino]-indan-2-carboxylic acid

https://huagongshe.com/reaction/1047771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[2-(-1-Ethyl-but-1-enyl)-3-methyl-benzoylamino]-indan-2-carboxylic acidHCID 68589661—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-[2-(1-Ethyl-butyl)-3-methyl-benzoylamino]-indan-2-carboxylic acidHCID 2516041228%

Reaction Steps

To a solution of 2-[2-(-1-ethyl-but-1-enyl)-3-methyl-benzoylamino]-indan-2-carboxylic acid ethyl ester (129) (270 mg, 0.72 mmol) in absolute EtOH (15 mL) is added the catalyst, Pd—C (50% wetted powder, 10% Pd, 46 mg, 2.2% mmol) under argon. The resulting reaction mixture is moved to the Paar apparatus to run hydrogenation: 50 psi, 70° C., overnight. The catalyst is removed by the filtration through a pre-column (10 g silica gel) and washed by EtOH. The combined EtOH solution is concentrated in vacuo. The residue is purified by HPLC to give a pure product (130) as white solid (75 mg, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-782c1c68e126403bace2e5a06958cf06
Source noteuspto-grants-2013_10