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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725927Generated: October 30, 2026

2,6-Di-tert-butyl-4-methylphenol → HCID 19710197, compound

https://huagongshe.com/reaction/725927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantLithium ChlorideHCID 433294—
ReactantEthynyltributyltinHCID 621176—
ReactantHCID 19710221HCID 19710221—
ReactantHCID 22468310HCID 22468310—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
ProductHCID 19710197HCID 19710197—

Reaction Steps

To a solution of 5-trifluoromethanesulfonyloxy-2-(di-n-propylamino)indan (Example 2) in 1,4-dixoane is treated with tri-n-butylethynylstannane, lithium chloride, tetrakis(triphenylphosphlne)palladium(0), and a few crystals of 2,6-di-tert-butyl-4-methylphenol under nitrogen (J. Am. Chem. Soc. 1987, 109, 5478). The mixture is refluxed for 6 h, cooled to room temperature, and treated with pyridine and pyridine fluoride and iluted with diethyl ether. The resulting crude product is purified by chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708018
Source datasetuspto-grants-1998_01
ORD IDord-8a0ee0b2273545a9bad4e13a2ffb1522
Source noteuspto-grants-1998_01