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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486400Generated: October 30, 2026

Acetonitrile → HCID 15233540, compound

https://huagongshe.com/reaction/486400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDichloromethaneHCID 6344—
ReactantPotassium PersulfateHCID 24412—
ReactantHCID 15233539HCID 15233539—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
ProductHCID 15233540HCID 15233540—

Reaction Steps

The 1,1,2,3,3,4-hexamethyl-6-methoxyindane (10.8 g) is then heated with copper(II) sulfate pentahydrate (18.04 g) and potassium peroxydisulfate (60.55 g) in acetonitrile and water (1:1, 500 ml) at reflux for about 15 to 20 minutes, following procedures similar to those described in Hauser et al., Synthesis, pp. 723-724 (1987). The mixture is then cooled to room temperature and methylene chloride (150 ml) is added. The layers are separated and the aqueous phase is further extracted with additional methylene chloride (2×70 ml). The combined organic solutions are dried with anhydrous sodium sulfate, filtered, and evaporated at reduced pressure to yield 5-formyl-1,1,2,3,3,4-hexamethyl-6-methoxyindane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292720
Source datasetuspto-grants-1994_03
ORD IDord-854cdd26e9124b20a77b3a76377e8c10
Source noteuspto-grants-1994_03