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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083869Generated: November 1, 2026

HCID 10566532, compound → HCID 22731781, compound

https://huagongshe.com/reaction/2083869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10566532HCID 10566532—
ReactantHCID 86584360HCID 86584360—
ProductHCID 22731781HCID 2273178186%

Reaction Steps

1-Benzenesulfonyl-5-chloro-2-methylindole prepared in accordance with the literature (J. Org. Chem., 47, 757 (1982) was reacted with Ac2O/AlCl3 in a similar manner described in Reference example 2 (3) to give 3-acetyl-1-benzenesulfonyl-5-chloro-2-methylindole. Yield: 86%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716605B2
Source datasetuspto-grants-2004_04
ORD IDord-4e2465c160c2486f97a54a7b5585b8d1
Source noteuspto-grants-2004_04