Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1,2-Bis(bromomethyl)-4-(trifluoromethyl)benzene | HCID 12601893 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 66878234 | HCID 66878234 | — |
Reaction Steps
Sodium (1.12 g, 48.6 mmol) was added to ethanol (16 mL). The solution was heated to reflux until all sodium was dissolved. To this solution was added diethyl malonate (3.71 g, 23.19 mmol) in ether (45 mL) and the above 1,2-bis-bromomethyl-4-trifluoromethylbenzene (7.7 g, 23.19 mmol) in ether (45 mL). The mixture was refluxed for 16 hrs and the precipitate was filtered out. The filtrate was evaporated and the residue was treated with water (35 mL) and potassium hydroxide (5.30 g). The mixture was stirred and refluxed for 5 hrs and treated with water (20 mL). The resulting mixture was extracted with ether (50 mL). The aqueous phase was acidified with concentrated hydrochloric acid and cooled in an ice bath. Solids were filtered and washed with water. After air drying, 5-trifluoromethyl-indan-2,2-dicarboxylic acid was obtained (3.08 g). LC-MS showed a single peak, C12H19F3O4 (m/e) calcd 274.0453, obsd 273.0 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07652053B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-6a21bbfba77b4aada355fa348c459ffa |
|---|
| Source note | uspto-grants-2010_01 |
|---|