HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-2-butene → 1-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Phosphate, Monobasic, Monohydrate | HCID 516949 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | 1-(2-Bromo-4-pyridinyl)cyclopropanecarboxaldehyde | HCID 86672756 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056858B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-894c9cbae3ce4e32a02f16eef2964d4d |
| Source note | uspto-grants-2015_06 |