HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4,4,4-Trifluoro-1-[4-(2-furyl)-3-methylphenyl]butane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-[4-(2-Furyl)-3-methylphenyl]ethanone | HCID 22316633 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4,4,4-Trifluoro-1-[4-(2-furyl)-3-methylphenyl]butane-1,3-dione | HCID 22316748 | — |
Reaction Steps
To a stirred solution of ethyl trifluoroacetate (0.66 g, 4.67 mmol) in t-butylmethylether (15 mL) was added sodium methoxide (28 wt. % solution in methanol; 1.2 mL, 4.98 mmol) over 2 min. A solution of 1-[4-(2-furyl)-3-methylphenyl]ethanone in t-butylmethylether (4 mL) was added dropwise over 5 minutes, and the mixture was stirred for 20 hours. 2N HCl (10 mL) was added, and the whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give 1.12 g of brown oil. The compound was used for next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294558B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-9130678ffac7440fb60723bc00b3ec4c |
| Source note | uspto-grants-2001_09 |