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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083867Generated: November 1, 2026

Acetic Anhydride → HCID 23552950, compound

https://huagongshe.com/reaction/2083867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6-chloroacetoxy-1-pivaloylindoleHCID 10379664—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 23552950HCID 2355295036%

Reaction Steps

To a suspension of 9.5 g (72 mmol) of aluminum chloride in dichloroethane (47.5 ml) was added dropwise 3.64 g (36 mmol) of acetic anhydride. After stirring for 15 min at room temperature, to the above mixture was added dropwise 3.3 g (11 mmol) of 6-chloroacetoxy-1-pivaloylindole (prepared in accordance with the literature (SYNTHESIS, p1018, 1994) in dichloroethane (33 ml). After stirring for 1 hour at room temperature, the mixture was poured into ice-water. The mixture was extracted with ethyl acetate. The extract was washed twice with water and aqueous sodium bicarbonate, and dried. The solution was concentrated and the obtained residue was chromatographed on silica gel (ethyl acetate as eluant) to give 1.23 g of 3-acetyl-6-chloroacetoxy-1-pivaloylindole as an oil. Yield: 36%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716605B2
Source datasetuspto-grants-2004_04
ORD IDord-bb957825af3c48c083763115a12bdd32
Source noteuspto-grants-2004_04