Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-tert-Pentylphenol | HCID 6643 | — |
| Reactant | HCID 178445677 | HCID 178445677 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178442192 | HCID 178442192 | 57% |
Reaction Steps
41 3 ml (0.55 mole) of 37% strength aqueous formaldehyde solution, 85.3 g (0.55 mole) of trans-4-tertbutylcyclohexylamine, 95 g (0.579 mole) of 4-tert-pentylphenol and 1 g of sodium hydroxide are added in succession to 300 ml of dioxane at from 20° to 35° C. The mixture is then stirred for 6 hours at 70° C. and cooled to +5° C., and the precipitate is filtered off under suction, washed with 100 ml of water and then with 50 ml of dioxane and dried. 104 g (57% of theory) of trans-2-(4'-tert-butylcyclohexylamino)-methyl-4-tert-pentylphenol are obtained as white crystals of melting point 148°-150° C. (active ingredient No. 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05019598 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-a2de1a0b92da42a482f9a54ed17d3e60 |
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| Source note | uspto-grants-1991_05 |
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