HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50494Generated: October 25, 2026
1-Diethoxyphosphorylpropan-2-one → 4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-one
https://huagongshe.com/reaction/50494
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Diethoxyphosphorylpropan-2-one | HCID 14028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Trifluoromethoxy)benzaldehyde | HCID 605139 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(Trifluoromethoxy)phenyl]-3-buten-2-one | HCID 69344118 | 54% |
Reaction Steps
EX-626A) Tetrabutylammonium iodide (0.4 g, 0.05 mol) was added to a well-stirred biphasic mixture of 12 mL of 50% NaOH and 20 mL of methylene chloride under a nitrogen atmosphere. A solution of 3-trifluoromethoxybenzaldehyde (4.0 g, 0.021 mol) and diethyl (2-oxopropyl)phosphonate (4.08 g, 0.021 mol) in 4.0 mL of methylene chloride was added dropwise to the stirred solution. The resulting mixture was stirred at room temperature for 15 min, then quenched with water and extracted with hexane. The hexane layer was dried over MgSO4. The crude product was purified by flash column chromatography on silica gel eluting with 1:10 ethyl acetate in hexane to give 2.6 g (54%) of the desired 4-[3-(trifluoromethoxy)phenyl]-3-buten-2-one product as a yellow oil. 1H NMR (CDCl3) δ 7.43 (m, 4H), 7.20 (d, 1H), 6.65 (d, 2H), 2.29 (s, 3H). 19F NMR (CDCl3) δ −62.05 (s, 3F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06710089B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-c4008e2f0b904dba885c659f391d9ec7 |
|---|
| Source note | uspto-grants-2004_03 |
|---|