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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582632Generated: November 1, 2026

Acetic Anhydride → Ethyl 5-acetoxyindole-2-carboxylate

https://huagongshe.com/reaction/1582632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl 5-hydroxy-1H-indole-2-carboxylateHCID 90677—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductEthyl 5-acetoxyindole-2-carboxylateHCID 11379620100%

Reaction Steps

A stirred solution of ethyl 5-hydroxyindole-2-carboxylate (7.79 g) and 4-dimethylaminopyridine (20 mg) in acetic anhydride (80 ml) was heated at 80° C. for 4 hours. The reaction was concentrated in vacuo and the residue was dissolved in ethyl acetate. Combined organic extracts were washed with hydrochloric acid (2 M), saturated aqueous sodium hydrogen carbonate solution, water, aqueous saturated sodium chloride solution and dried. The solution was concentrated in vacuo to yield the product as a yellow solid (9.39 g,100%). NMR: δ 1.20 (t, 3H), 2.10 (s, 3H), 4.19 (q, 2H), 6.86 (dd, 1H), 6.97 (d, 1H), 7.20 (s, 1H), 7.29 (d, 1H); m/z 248 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737435B1
Source datasetuspto-grants-2004_05
ORD IDord-0270d477703d45aaadb9a8c1cd2f9e89
Source noteuspto-grants-2004_05