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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172965Generated: October 30, 2026

2-Methyl-2-butene → 1-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acid

https://huagongshe.com/reaction/2172965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium Phosphate, Monobasic, MonohydrateHCID 516949—
ReactantSodium ChloriteHCID 23668197—
Reactant1-(2-Bromo-4-pyridinyl)cyclopropanecarboxaldehydeHCID 86672756—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product1-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acidHCID 71743246—

Reaction Steps

A solution of sodium chlorite (368 mg, 3.26 mmol) and sodium dihydrogen phosphate monohydrate (449 mg, 3.26 mmol) in 5 mL of water is added dropwise to a solution of crude 1-(2-bromo-pyridin-4-yl)-cyclopropanecarbaldehyde (566 mg, 2.50 mmol) and 2-methyl-2-butene (1.73 mL, 16.3 mmol) in tert-butanol (12 mL), and the resulting reaction mixture is stirred at room temperature. After 18 hours, the mixture is concentrated in vacuo, acidified to pH 2 with 1M aqueous solution of HCl, diluted with brine (25 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers are dried over Na2SO4, filtered and concentrated to afford crude 1-(2-bromo-pyridin-4-yl)-cyclopropanecarboxylic acid, which is used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056858B2
Source datasetuspto-grants-2015_06
ORD IDord-894c9cbae3ce4e32a02f16eef2964d4d
Source noteuspto-grants-2015_06