HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 86660320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86660321 | HCID 86660321 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86660320 | HCID 86660320 | — |
Reaction Steps
Triethylamine 270 mg was added under room temperature to a THF 10 mL solution containing 1,7-bis(4′-hydroxy-3′-trifluoromethoxyphenyl)-4-methoxycarbonylethyl 1,6-heptadiene 3,5-dione 500 mg and acetic anhydride 272 mg, and the resultant solution was agitated for 2 hours at room temperature. After the reaction was ended, water was poured, and the resultant solution was subjected to extraction with ethyl acetate. The extract was dried with sodium sulfate, and the solvent was removed. The crystal residue was washed with a small quantity of ethanol, filtered, and dried, whereby 430 mg of 1,7-bis(4′-acetoxy-3′-trifluoromethoxyphenyl)-4-methoxycarbonylethyl-1,6-heptadiene-3,5-dione having a melting point of 149 to 150° C. was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08956589B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-20cfd927a22645a4b73c7073dc782833 |
| Source note | uspto-grants-2015_02 |