HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → (E)-4-(2,4-difluorophenyl)but-3-en-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-4-(2,4-difluorophenyl)but-3-en-2-one | HCID 58310994 | — |
Reaction Steps
To a mixture of 2,4-difluorobenzaldehyde (5.0 ml, 45.7 mmol) and acetone (10.75 ml, 146 mmol) in Water (10 ml), was added 0.25M sodium hydroxide (18.30 ml, 4.57 mmol). The reaction mixture was heated to for 2 h. The mixture was poured into ice water. It was extracted with ethyl acetate (200 ml). The organic layer was dried, filtered, and evaporated to give (E)-4-(2,4-difluorophenyl)but-3-en-2-one as yellow oil. It was used for the next reaction without purification. 1H NMR (CDCl3/400 MHz): δ (ppm) 7.60 (d, 1H), 7.60-7.53 (m, 1H), 6.96-6.86 (m, 2H), 6.73 (d, 1H), 2.39 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08674115B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-5185cd3713a448b7a379a6b0f8ac835b |
| Source note | uspto-grants-2014_03 |