HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 5709173, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloro-6-fluorobenzaldehyde | HCID 67847 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 5709173 | HCID 5709173 | 51.8% |
Reaction Steps
(72) To a solution of the 2-chloro-6-fluoro-benzaldehyde (1.59 g, 10.0 mmol) and acetone (290 mg, 5.00 mmol) in 15 ml of ethanol was added 5 ml of 40% potassium hydroxide at 10° C. After stirring for several hours at room temperature, the solution was filtered. The precipitate was recrystallized from ethanol to afford 879 mg (51.7%) of a light-yellow powder: mp 143.5-144.3° C. 1H NMR (250 MHz) δ 7.98-7.91 (d, 2H), 7.36-7.22 (m, 6H), 7.13-7.03 (m, 2H); 13C NMR (62.7 MHz) 189.6, 134.0, 132.1, 131.8, 131.2, 131.0, 126.3, 115.4, 115.0 ppm. Elemental Analysis. Calculated for C17H10Cl2F2O5: C, 60.20; H, 2.98. Found: C, 60.07; H, 2.99.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462075B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-888c68cc26df4675b89c6818f6b2e8db |
| Source note | uspto-grants-2002_10 |