Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642528Generated: November 1, 2026

Acetic Anhydride → 1-Acetyl-4-bromo-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/1642528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Bromo-1H-indole-3-carbaldehydeHCID 2763178—
Product1-Acetyl-4-bromo-1H-indole-3-carbaldehydeHCID 5341578874%

Reaction Steps

4-Bromo-1H-indole-3-carbaldehyde (4.0 g, 17.8 mmol) was stirred in acetic anhydride (20 mL) at reflux for 4 h. The reaction was cooled and concentrated in vacuo. Cold MeOH was added to precipitate a white solid, which was collected by filtration to give 3.5 g (74%) of 1-acetyl-4-bromo-1H-indole-3-carbaldehyde. MS (ES) [m+H] calc'd for C11H8BrNO2, 266, 268; found 266, 268.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119655B2
Source datasetuspto-grants-2012_02
ORD IDord-855426df7db447ce9db464b7678926c2
Source noteuspto-grants-2012_02