HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cinnamoylbenzene → ethyl 2-[(E)-3-(1,2,3,4-tetrahydro-1,4a,9b-trimethyl-1,4-methanodibenzofuran-8-yl)-3-oxo-1-propenyl]-4-thiophenecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cinnamoylbenzene | HCID 7189 | — |
| Reactant | 1,2,3,4-Tetrahydro-1,4a,9b-trimethyl-1,4methanodibenzofuran-8-yl methyl ketone | HCID 15344130 | — |
| Reactant | Ethyl 5-formylthiophene-3-carboxylate | HCID 18789515 | — |
| Product | ethyl 2-[(E)-3-(1,2,3,4-tetrahydro-1,4a,9b-trimethyl-1,4-methanodibenzofuran-8-yl)-3-oxo-1-propenyl]-4-thiophenecarboxylate | HCID 18925572 | — |
Reaction Steps
2.70 g (10 mmol) of the methyl ketone obtained in Example 3 were converted to chalcone in the presence of 1.7 g of 4-(ethoxycarbonyl)thiophenecarbaldehyde under the conditions described in Example 8 to yield, after recrystallization in ethyl acetate, 2.2 g (52%) of the expected compound, melting at 149°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747530 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-8430838696bc4e42921f499721e3f866 |
| Source note | uspto-grants-1998_05 |