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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582650Generated: November 1, 2026

Acetic Anhydride → N-(3,4-Dichlorobenzyl)-5-acetoxyindole-2-carboxylic acid

https://huagongshe.com/reaction/1582650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantN-(3,4-Dichlorobenzyl)-5-hydroxyindole-2-carboxylic acidHCID 9949615—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
ProductN-(3,4-Dichlorobenzyl)-5-acetoxyindole-2-carboxylic acidHCID 22718737—

Reaction Steps

To a solution of N-(3,4-Dichlorobenzyl)-5-hydroxyindole-2-carboxylic acid (10 g) in warm ethyl acetate (250 ml) was added 4-dimethylaminopyridine (100 mg) and acetic anhydride (5.0 ml) and the resulting mixture was stirred for 2 hours. The organics were washed with 1N HCl and dried. Hexane was added to cause crystallision of the product. The solid was filtered and washed with hexane to give the desired product. (5 g, 44%). 1H NMR (DMSO-d6) δ 2.25 (s, 3H), 5.85 (s, 2H), 6.9 (dd, 1H), 7.05 (dd, 1H), 7.3-7.6 (m, 5H); m/z 378, 380 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737435B1
Source datasetuspto-grants-2004_05
ORD IDord-8f74b749bf5d4e83a3d8fe9045f41b9c
Source noteuspto-grants-2004_05