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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258048Generated: October 30, 2026

Chloride → HCID 54394949, compound

https://huagongshe.com/reaction/258048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantDimethylformamideHCID 6228—
Reactant6-methoxy-2,3-dihydro-1H-indene-5-carboxylic acidHCID 19936571—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54394949HCID 54394949—

Reaction Steps

To a mixture of 5-methoxyindan-6-carboxylic acid (3.84 g), DMF (0.1 ml) and tetrahydrofuran (50 ml) was added oxyalyl chloride (2.1 ml) dropwise. The mixture was stirred at room temperature for 1 hour, at the end of which time the solvent was distilled off to give 5-methoxyindan-6-carboxylic acid chloride. This chloride was dissolved in dichloromethane (50 ml) and after addition of 2,6-di-tert-butylphenol (4.12 g), tin tetrachloride (2.6 ml) was added dropwise with ice-cooling. The mixture was stirred under ice-cooling for 30 minutes and, then, poured in diluted hydrochloric acid. The organic layer was washed with water and dried (MgSO4) and the solvent was distilled off. To the residue was added ethanol-hexane to give crystals of 5-(3,5-di-tert-butyl-4-hyroxybenzoyl)-6-methoxyindan (4.23 g, 55.7%). Recrystallization from ethanol gave colorless prisms, m.p. 154°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264454
Source datasetuspto-grants-1993_11
ORD IDord-69261c2e7a9e4c019c9f5ba360758d79
Source noteuspto-grants-1993_11