HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cornforth reagent → 1-(5-Bromo-2-fluorophenyl)butan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | HCID 63894506 | HCID 63894506 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(5-Bromo-2-fluorophenyl)butan-1-one | HCID 52983815 | 75.1% |
Reaction Steps
To a solution of 1-(5-bromo-2-fluoro-phenyl)-butan-1-ol (6.2 g, 25 mmol) in dry CH2Cl2 (60 mL) were added pyridinium dichromate (19.0 g, 50.3 mmol) and molecular sieves powder (1.24 g) at room temperature and stirred overnight. The reaction mixture was filtered through diatomaceous earth and washed with diethyl ether (200 mL). The combined CH2Cl2 and ether layers were dried over anhydrous Na2SO4, filtered and concentrated to give a crude product, which was purified by column chromatography using 5% ethyl acetate/pet-ether as eluents to afford 1-(5-bromo-2-fluorophenyl)butan-1-one (4.6 g, 75%) as a syrup. 1H NMR (CDCl3): δ 8.0 (m, 1H), 7.5-7.6 (m, 1H), 7.0 (t, 1H), 2.9-3.0 (m, 2H), 1.7 (q, 2H), 1.0 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318762B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-6cd28482d45f45ab948fa08ae00df467 |
| Source note | uspto-grants-2012_11 |