HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → Acetic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | HCID 18184290 | HCID 18184290 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 18184320 | HCID 18184320 | — |
Reaction Steps
Malonic acid diethyl ester (8.5 g) was dissolved in dimethylformamide (75 mL) followed by addition of potassium tert-butoxide (5.9 g). After stirring for 15 min at room temperature, a solution of 3-chloromethyl-7-chloro-4-methylbenzofuran (3.8 g, prepared analogously to the 5-fluoro analogue as described in Example, 2) in dimethylformamide (25 mL) was added dropwise. After stirring for 2 hours the reaction mixture was poured onto ice-water. Standard work-up with acetyl acetate gave a yellow oil (10 g) of diethyl 2-(7-chloro-4-methylbenzofuran-3-yl)malonate, sufficiently pure for further synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596722B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-49399576c1e94afbb99904f1588247f7 |
| Source note | uspto-grants-2003_07 |