HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585862Generated: November 2, 2026
Water → 1H-Indene, 2,3-dihydro-1,3-dimethyl-1-(2-methyl-2-phenylpropyl)-3-phenyl-
https://huagongshe.com/reaction/1585862
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Alpha-Methylstyrene | HCID 7407 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1H-Indene, 2,3-dihydro-1,3-dimethyl-1-(2-methyl-2-phenylpropyl)-3-phenyl- | HCID 170585 | 46.6% |
Reaction Steps
To a four-necked 2000 ml-volume flask equipped with a stirring machine, a dropping funnel, a Dimroth condenser and a thermometer, there was added a solution of 300.4 g of α-methylstyrene in 1200 g of toluene, followed by setting the temperature thereof to 0° C. by dipping the flask in ice-water and gradual dropwise addition of 300 ml of a toluene solution containing a catalyst, i.e., 1.02 g AlCl3 -2.5 ml CH3NO3 to the contents of the flask with stirring. The reaction solution at the completion of the reaction-was colored pale yellow. After the completion of the reaction, water was gently dropwise added to the reaction system to thus decompose the catalyst. Then the organic phase was washed with water, dried and concentrated. Further the organic phase was subjected to vacuum distillation under a degree of vacuum of 670 Pa and at a temperature ranging from 218 to 221° C. to give 140.0 g of 1,3-dimethyl-3-phenyl-1-(2-methyl-2-phenylpropyl) indane (MPI).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05939593 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-1f8b2d481ed744a9bd7d8ab03d791111 |
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| Source note | uspto-grants-1999_08 |
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