Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67915896 | HCID 67915896 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67915919 | HCID 67915919 | — |
Reaction Steps
(3aRS,7aRS)-7,7-Bis(3-tolyl)-2-vinyloxycarbonylperhydro-4-isoindolone (7.4 g) is treated with a 6N solution (39 cc) of hydrochloric acid in dioxane for 30 minutes at 25° C. The solution is concentrated to dryness under reduced pressure (2.7 kPa) and the residue taken up with ethanol (100 cc). The solution is heated to 60° C. for 2 hours and stirred for 16 hours at 25° C., then concentrated to dryness under reduced pressure (2.7 kPa). The residue is solidified with isopropyl ether and the solid is washed, drained and dried. 7,7-Bis(3-tolyl)perhydro-4-isoindolone hydrochloride (6.36 g) is obtained in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112988 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-18af885dff45472fb5c13de652118b94 |
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| Source note | uspto-grants-1992_05 |
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