HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydrofuran → HCID 66735283, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 66735592 | HCID 66735592 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66735283 | HCID 66735283 | 40.7% |
Reaction Steps
To a solution of 0.25 g of 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid amide that was synthesized under Synthetic Example 9 in 3 mL of dichloromethane, 68 mg of 2,3-dihydrofuran and a catalytic amount of p-toluenesulfonic acid monohydrate were added and the mixture was stirred for 18 hours at room temperature. The solvent was distilled off from the reaction solution under reduced pressure, and the resulting residue was purified using silica gel column chromatography that was eluted with ethyl acetate-hexane (2:3) followed by crystallization from a mixed solvent of hexane and a small amount of ethyl acetate to obtain 0.12 g of aimed product as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700808B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-54e0e0e88d89496ea2a66552cf447732 |
| Source note | uspto-grants-2010_04 |