Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 178511237 | HCID 178511237 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178511239 | HCID 178511239 | 77.8% |
Reaction Steps
3.0 g of crude trans-4-[trans-4-[2-(I.3-dioxolan-2-yl)ethyl]cyclohexyl)cyclohexanecarbonitrile were suspended in 50 ml of water, 25 ml of glacial acetic acid and 10 ml of dioxan while gassing with argon and stirred at 100° C. for 1 hour. Thereafter, the reaction solution was treated with 100 ml of water. The aqueous phase was separated and extracted three times with 100 ml of diethyl ether each time. The organic phases were washed with 100 ml of dilute sodium hydrogen carbonate solution and with 100 ml of water, dried over magnesium sulfate, filtered and concentrated. Recrystallization of the yellow crystals obtained (2.25 g) from 60 ml of hexane gave 1.98 g of 3-[trans-4-(trans-4-cyanocyclohexyl)cyclohexyl]-propionaldehyde as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302317 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-522cd3bd8e9143638243038ced282780 |
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| Source note | uspto-grants-1994_04 |
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