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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857688Generated: October 31, 2026

2,6-Di-tert-butyl-4-methylphenol → HCID 21865309, compound

https://huagongshe.com/reaction/857688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 58759740HCID 58759740—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21865309HCID 21865309—

Reaction Steps

To a solution of trifluoromethanesulfonic acid 2-[6-(quinolin-7-yloxy)-pyrimidin-4-yl]-5-trifluoromethyl-phenyl ester, (Example 192(a)), (600 mg, 1.2 mmol) in dioxane (6.0 mL) was added vinyltributylstannate (370 μL, 1.6 mmol, Fluka), LiCl (150 mg, 3.5 mmol, Aldrich), Pd(PPh3)4 (27 mg, 0.02 mmol, Strem) and a few crystals of 2,6-di-tert-butyl-4-methylphenol (Aldrich). The reaction mixture was stirred at reflux for 21 h. The resulting mixture was allowed to cool to room temperature and concentrated in vacuum. Purification by silica gel chromatography (1% MeOH/CH2Cl2) provided the title compound as a white amorphous solid. MS (ESI, pos. ion) m/z: 394 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144888B2
Source datasetuspto-grants-2006_12
ORD IDord-3fd544a951164c1bb45bfbc377e3732f
Source noteuspto-grants-2006_12