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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515160Generated: October 30, 2026

2-Methyl-2-butene → 4-Bromo-2-methoxy-6-methylbenzoic acid

https://huagongshe.com/reaction/515160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
Reactant4-Bromo-2-methoxy-6-methylbenzaldehydeHCID 45480385—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product4-Bromo-2-methoxy-6-methylbenzoic acidHCID 4548038690%

Reaction Steps

To a suspension of 4-bromo-2-methoxy-6-methyl-benzaldehyde (1.25 g, 5.45 mmol) in tert-butanol (21.7 ml) is added a solution of sodium chlorite (0.98 g, 10.9 mmol) and monosodium phosphate (4.25 g, 27.3 mmol) in water (11 ml). To the solution is added 2-methyl-2-butene (4.63 ml, 43.7 mmol). The resulting homogeneous solution is stirred at RT for 30 min. After completion of the reaction, the solvent is evaporated and the residue is diluted with water and acidified with 1 M hydrochloric acid to pH=1 and extracted with methyl tert-butyl ether (3×40 ml). The combined organic layers are extracted with 1 M sodium hydroxide solution which is further acidified with 6 M hydrochloric acid and extracted with ethyl acetate (3×50 ml). The organic layer is washed with brine (40 ml), dried over sodium sulfate and concentrated to yield 4-bromo-2-methoxy-6-methyl-benzoic acid (1.2 g, 4.89 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-59d2fc30d3cf4f7698d9e9e835731d24
Source noteuspto-grants-2015_08