Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Benzene, 1-chloro-2-(1-methylethyl)- | HCID 16377 | — |
| Reactant | HCID 10968208 | HCID 10968208 | — |
| Product | 1-Methyl-3-phenylindane | HCID 22924 | — |
| Product | HCID 21490570 | HCID 21490570 | — |
Reaction Steps
A mixture of 375 parts of phosphoric acid (95% strength by weight) and 1 part of phenothiazine is irradiated for 10 minutes analogously to Example 11. A mixture of 52 parts of styrene, 76 parts of α-methyl-o-chlorostyrene and 94 parts of o-chloro-isopropylbenzene is added to the irradiated solution over 4 hours at 35° to 40° C. After completion of the addition, the mixture is stirred for a further hour at 40° C. The organic phase is separated off and washed with 150 parts of 5 per cent strength by weight sodium hydroxide solution, and fractional distillation gives 20 parts of 1-methyl-3-phenylindan and 68 parts of 1,3-dimethyl-3-(o-chlorophenyl)-indan (b.p. 147° to 152° C (0.4 mm)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998894 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-39fec260c9134dea8777484c293dc207 |
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| Source note | uspto-grants-1976_12 |
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