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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352352Generated: October 30, 2026

2-Methyl-2-butene → 2-Difluoromethyloxy-4,6-dimethylphenyl acetic acid

https://huagongshe.com/reaction/352352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
Reactant2-Difluoromethyloxy-4,6-dimethylphenylacetaldehydeHCID 18684693—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product2-Difluoromethyloxy-4,6-dimethylphenyl acetic acidHCID 2270932914%

Reaction Steps

19.2 g of 2-difluoromethyloxy-4,6-dimethylphenylacetaldehyde (XXXIV-c-1) as the crude product were dissolved in 270 ml of tert-butanol, the solution was mixed with 90.4 g of 2-methyl-2-butene, and a solution of 90 g of sodium dihydrogen phosphate and 42 g of sodium chlorite in 353 ml of water was subsequently added dropwise at room temperature. The mixture was stirred for four hours and then stirred into 400 ml of ethyl acetate, and the phases were separated. The aqueous phase was extracted two more times using ethyl acetate, and the combined organic phases were dried over magnesium sulphate and concentrated. After stirring with hexane, 11 g of solid were isolated, from which 2.5 g (14% of theory via 2 steps) of 2-difluoromethyloxy-4,6-dimethylphenylacetic acid of melting point 124-127° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06746990B2
Source datasetuspto-grants-2004_06
ORD IDord-791c1f8aa2a6468f94d242303c753131
Source noteuspto-grants-2004_06