Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium tritertbutoxyaluminohydride | HCID 16684435 | — |
| Reactant | HCID 54136437 | HCID 54136437 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14835753 | HCID 14835753 | — |
Reaction Steps
3-Methoxycarbonylcinnamyl chloride (24 g) was dissolved in dry tetrahedrofuran and then this solution added to lithium tri-tert-butoxyaluminohydride (63.5 g) dissolved in tetrahydrofuran (250 ml) at -78° C. The resultant clear solution was stirred at -78° C. for 30 minutes then it was added to ice and 2 M hydrochloric acid (750 ml). The two phase mixture was extracted 4 times with dichloromethane. After drying the dichloromethane was evaporated to yield the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04963578 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-73c4eb5c5ed0445ea5731c9527b3c68e |
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| Source note | uspto-grants-1990_10 |
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