HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423518Generated: November 2, 2026
1-(5-Bromo-2-nitrophenyl)ethan-1-ol → 1-(5-Bromo-2-nitrophenyl)ethanone
https://huagongshe.com/reaction/2423518
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(5-Bromo-2-nitrophenyl)ethan-1-ol | HCID 45073390 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(5-Bromo-2-nitrophenyl)ethanone | HCID 12224157 | 77% |
Reaction Steps
Jones Reagent (2.67 M, 2.54 mL, 6.79 mmol) was added dropwise to 1-(5-bromo-2-nitrophenyl)-ethanol (1.67 g, 6.79 mmol) in acetone (34 mL) at 0° C., then the reaction mixture was stirred for 10 minutes. Any excess Jones reagent was quenched by the addition of iso-propanol, then the reaction mixture was neutralized with saturated sodium bicarbonate, and the acetone was removed by evaporation. Water was added and the solution was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, then filtered and concentrated. The residue was purified by silica gel chromatography eluting with 1:9 ethyl acetate:hexanes to give 1.27 g (77%) of 1-(5-bromo-2-nitrophenyl)-ethanone as a solid. 1H NMR (400 MHz, d6-DMSO): δ 8.05 (d, J=5 Hz, 1H), 8.04 (s, 1H), 7.96 (dd, J=9, 2 Hz, 1H), 2.57 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960552B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-65099191847e4dec8488c819bda6cb39 |
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| Source note | uspto-grants-2011_06 |
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