HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → Methyl 3-(3-fluorophenyl)prop-2-ynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 1-(2,2-Dibromoethenyl)-3-fluorobenzene | HCID 22562336 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Methyl 3-(3-fluorophenyl)prop-2-ynoate | HCID 54395407 | 110.3% |
Reaction Steps
To a stirred solution of 1-(2,2-dibromo-vinyl)-3-fluoro-benzene (23.8 g) in anhydrous THF (350 ml) cooled to −78° was added dropwise over 30 minutes, n-butyllithium (2.2 eq, 1.6M in hexanes). The mixture was stirred for a further 30 minutes at −78° before methyl chloroformate (11.6 g, 9.5 ml) was added and the resultant mixture allowed to warm to 0° for 1 hour before being diluted with 1:1 saturated aqueous sodium bicarbonate:ammonium chloride (100 ml) and extracted into ether (2×100 ml). The combined organic extract was washed with brine (25 ml), dried (Na2SO4) and evaporated to dryness to give the title compound as a brown oil (16.7 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451794B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-f0fb45e20bd54216a92a038f5a16ce54 |
| Source note | uspto-grants-2002_09 |