Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 70622813 | HCID 70622813 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54401717 | HCID 54401717 | 90% |
Reaction Steps
To a slurry of 15.0 g (0.395 mole) of LiAlH4 and 500 ml of anhydrous ether in a 5 liter, 3-necked flask fitted with a condenser, mechanical stirrer and dropping funnel was added 20.0 g (0.084 mole) of 4,5-dimethoxy-7-nitrovinylindane dissolved in 2 liters of ether. The addition was made over a period of about 4 hours while refluxing the ether slurry. When the addition was completed, refluxing was continued for an additional 1 to 2 hours. After the addition of 20 g of diatomaceous earth and then 70 ml of water slowly, dropwise, with cooling in an ice bath, the supernatant ether was decanted, the salts were washed with fresh ether several times followed by decantation and finally filtration. The solvent was removed by distillation and more thoroughly on a rotary evaporator. Cooling in an ice bath gave 15.91 g (90 percent) of 4,5-dimethoxy-7-aminoethylindane as a slightly yellow solid, m.p., 45°-48° C. High vacuum distillation gave an analytical sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03954774 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-c748796bb1a046fc856283762c6c7598 |
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| Source note | uspto-grants-1976_05 |
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