HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoroacetophenone → 3-Fluorophenacyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoroacetophenone | HCID 9967 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Fluorophenacyl bromide | HCID 2737451 | — |
Reaction Steps
A solution of 1-(3-fluorophenyl)ethanone (14.0 g, 100 mmol) (Aldrich) in dioxane (250 mL) at 12-15° C. was treated with a solution of bromine (17 g, 105 mmol) in dioxane (120 mL) drop wise over 0.5 h. This was stirred for 15 min and most of the solvent removed. The residue was taken up in hexane (200 mL), washed 2× water, and dried (MgSO4). Solvent was removed to give 2-bromo-1-(3-fluorophenyl)ethanone. 1H NMR (CDCl3), 300 MHz) δ3.71 (s, 2H, CH2), 7.30-7.77(m, 4H, Aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423053B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-b5a4959aa8414c598e9a19d8cf9c0e80 |
| Source note | uspto-grants-2008_09 |