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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056004Generated: November 2, 2026

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

https://huagongshe.com/reaction/2056004

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 numberUS07332511B2
Source datasetuspto-grants-2008_02
ORD IDord-72d831ed63144a42b35c9b7c6635921d
Source noteuspto-grants-2008_02