HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl malonate → Dimethyl 4-nitro-1H-indene-2,2(3H)-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1,2-Bis(bromomethyl)-3-nitrobenzene | HCID 12317751 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Dimethyl 4-nitro-1H-indene-2,2(3H)-dicarboxylate | HCID 57565181 | 70.2% |
Reaction Steps
To a solution stirred under nitrogen at room temperature of 5.0 mL methanol in 15.0 mL ether was added 0.84 g 60% sodium hydride (0.021 mol) in small portions (sodium hydride was used because metallic sodium was not available). After the addition was complete, the nearly clear and colorless solution was stirred for 5 minutes. To it was then added 1.3 g dimethyl malonate, giving a slightly cloudy colorless solution. To this was rapidly added a suspension of 3.1 g 1,2-bis(bromomethyl)3-nitrobenzene, which immediate gave a precipitate suspended in a dark green solution. This was removed by filtation and the filtrate was concentrated. The residue was purified on silica (20%-100% CH2Cl2 in hexanes) to give 1.93 g off-white solid (67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863276B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-3333ab496f664a3aab3644d8d1b651ee |
| Source note | uspto-grants-2011_01 |