HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → 2,2-Dicarboethoxy-indane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | o-Bis(bromomethyl)benzene | HCID 66665 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2-Dicarboethoxy-indane | HCID 11010777 | 74% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
Dissolve diethyl malonate (7.6 mL, 50 mmol) in anhydrous tetrahydrofuran (500 mL) and place under an argon atmosphere. Cool to 5° C., add sodium hydride (1.2 g, 50 mmol) and stir briefly until homogeneous. Add α,α'-dibromo-o-xylene (13.2 g, 50 mmol) and stir an additional 15 minutes. Add additional sodium hydride (1.2 g, 50 mmol) and stir for 16 hours while warming to room temperature. Filter, evaporate the solvent in vacuo and purify by silica gel chromatography (1:1 methylene chloride/hexane) to give 2,2-dicarboethoxyindan (9.64 g, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05486513 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-e0e47c15c0f547a1ab6a3066975746e9 |
| Source note | uspto-grants-1996_01 |