HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 23117342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | HCID 23117349 | HCID 23117349 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 23117342 | HCID 23117342 | — |
Reaction Steps
5 mL of trifluoromethanesulfonic anhydride was added under ice cooling to a 50 mL pyridine solution of 5 g of the compound obtained in Example 39, and the system was stirred for 2 hours at the same temperature. After the reaction, water was added at the same temperature, and extraction was performed with ethyl acetate. The extracted organic layer was washed with saturated brine, dried with magnesium sulfate, and then subjected to reduced-pressure solvent distillation. The residue thus obtained was refined by silica gel column chromatography (25% ethyl acetate/hexane) to obtain 6.24 g of 2-acetyl-4,5-dihydro-7-(trifluoromethanesulfonyloxy)naphtho[1,2-b]thiophene in the form of a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384974B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-8c312239f45b499e867b44b5ceb0fb4f |
| Source note | uspto-grants-2008_06 |