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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077306Generated: October 31, 2026

Acetic Anhydride → HCID 21503923, compound

https://huagongshe.com/reaction/1077306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Ethyl-9H-fluoreneHCID 274939—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 21503899HCID 21503899—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 21503923HCID 21503923—

Reaction Steps

2-Butylfluorene (6.1 g.) was acetylated exactly as described for 2-ethylfluorene in the preceding Example 21, using acetic anhydride (3.08 g.) and aluminium chloride (8.66 g.) in dichloroethane. The product was recrystallised from light petroleum to give 2-acetyl-7-butylfluorene, m.p. 102°-104.5°. This product (1.98 g.) was oxidised with sodium hypobromite (from 7.23 g. of bromine and 4.52 g. sodium hydroxide in 160 ml. water) exactly as described for 2-acetyl-7-ethylfluorene in the preceding Example. The 7-butylfluorenone-2-carboxylic acid thus isolated had m.p. > 300° and was homogeneous by thin layer chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959482
Source datasetuspto-grants-1976_05
ORD IDord-6b102e6e31f6401fbd8b3e0a86ff4063
Source noteuspto-grants-1976_05