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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505662Generated: November 1, 2026

2-Methyl-2-butene → 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzoic acid

https://huagongshe.com/reaction/505662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
Reactant2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehydeHCID 21669817—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzoic acidHCID 68717409112.8%

Reaction Steps

The above-obtained 2-(benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde (0.80 g, 2.3 mmol) was dissolved in tert-butyl alcohol (20 mL) and the obtained solution was added with 2-methyl-2-butene (10 mL, 94 mmol), sodium chlorite (2.0 g, 22 mmol), sodium dihydrogen phosphate (2.0 g, 17 mmol) and water (5 mL), followed by stirring at a room temperature for 10 hours. The reaction mixture was extracted with chloroform 3 times. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate. Then the solvent was evaporated under reduced pressure to obtain 2-(benzyloxymethyl)-4,6-bis(methoxymethoxy)benzoic acid (0.94 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781485B2
Source datasetuspto-grants-2010_08
ORD IDord-acfebf0766b54e6a9f1d4344baad0be6
Source noteuspto-grants-2010_08