HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide dimethyl acetal → 2-Dimethylaminomethylene-5-(2-methoxy-phenyl)-cyclohexane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 5-(4-Chlorophenyl)-2-[(dimethylamino)methylene]-1,3-cyclohexanedione | HCID 567070 | — |
| Reactant | 5-(2-Methoxyphenyl)-1,3-cyclohexanedione | HCID 17122313 | — |
| Product | 2-Dimethylaminomethylene-5-(2-methoxy-phenyl)-cyclohexane-1,3-dione | HCID 58269377 | — |
Reaction Steps
The title compound was prepared from 5-(2-methoxy-phenyl)-cyclohexane-1,3-dione (386 mg, 1.77 mmol), example 1/a, and N,N-dimethylformamide dimethylacetal (2 ml), following the procedure described for 5-(4-chloro-phenyl)-2-dimethylaminomethylene-cyclohexane-1,3-dione (example 2/a stage 1) except that the reaction was run at 100° C. for 2 h, after which the solvent was removed by evaporation under reduced pressure to produce the title compound as a brown oil. The title compound was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592430B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-7315d5875af74fd98f60a4d51d911152 |
| Source note | uspto-grants-2013_11 |