HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → (cis)-4-(3,4-Dimethoxyphenyl)-2-(2-(2-methoxyphenyl)-2-oxoethyl)-4a,5,6,7,8,8a-hexahydro-2H-phthalazin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | (cis)-4-(3,4-Dimethoxyphenyl)-4a,5,6,7,8,8a-hexahydro-2H-phthalazin-1-one | HCID 10913208 | — |
| Reactant | Methoxyphenacylbromide | HCID 15556716 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (cis)-4-(3,4-Dimethoxyphenyl)-2-(2-(2-methoxyphenyl)-2-oxoethyl)-4a,5,6,7,8,8a-hexahydro-2H-phthalazin-1-one | HCID 70303751 | — |
Reaction Steps
A mixture of 2 g of compound 1 and 1 eq sodium ethanolate in 30 ml of dimethylformamide was added to a solution of 2 g of ω-bromo-2-methoxyacetophenone in dimethylformamide. After 30 min small portions of additional ω-bromo-2-methoxyacetophenone (total 5 gram) and sodium ethanolate were added during 2 hours. Subsequently the reaction mixture was evaporated and the residue partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate and evaporated. The residue was purified by chromatography (dichloromethane). Crystallized from methanol. M.p. 93°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06103718 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-fd90fce93e6642029d77b77bc6ac9653 |
| Source note | uspto-grants-2000_08 |