Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Alpha-Methylstyrene | HCID 7407 | — |
| Edukt | Sodium Cyanate | HCID 517096 | — |
| Edukt | 2,6-Bis(2-isocyanatopropan-2-yl)naphthalene | HCID 20029335 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (1-Chloro-1-methylethyl)benzene | HCID 70281 | — |
Reaktionsschritte
α,α-Dimethylbenzylchloride was prepared by passing a stream of dry hydrogen chloride gas through a solution of methylene dichloride (750 ml.) and α-methylstyrene (500 g, 4.2 moles) at 4° C. The reaction and work-up were employed for the paration of 2,6-bis(1-isocyanato-1-methylethyl)naphthalene described in Example 4. The resulting monochloride was dissolved in 750 ml. methylene dichloride and was added to a cooled (4° C.) catalyst solution previously prepared from anhydrous, 90% sodium cyanate (389 g,5.39 moles), pyridine (50 ml., 0.633 mole), zinc chloride (39.15 g,0.28 mole) and 1 ml. H2O in 1075 ml methylene dichloride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04399074 |
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| Quelldatensatz | uspto-grants-1983_08 |
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| ORD ID | ord-2d2c6a269b1b428c9f05c425567213b9 |
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| Quellennotiz | uspto-grants-1983_08 |
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