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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277674Generated: October 30, 2026

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

https://huagongshe.com/reaction/277674

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 numberUS06358887B1
Source datasetuspto-grants-2002_03
ORD IDord-9f85cf0a0e9447d5ac7138907c46dfcd
Source noteuspto-grants-2002_03