HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501908Generated: October 29, 2026
p-Toluenesulfonic acid monohydrate → 5-methyl-1H-indene
https://huagongshe.com/reaction/501908
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 6-Methyl-2,3-dihydro-1H-inden-1-ol | HCID 12337217 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-methyl-1H-indene | HCID 81997 | — |
Reaction Steps
Sodium borohydride (1.3 g) was added to a solution of 6-methyl-indane-1-one (5.0 g) in methanol (50 ml) at 0° C., and the mixture was stirred for one hour. The reaction mixture was poured into ice-cooled water, and extracted with ethyl acetate. The organic layer was washed with saturated saline solution and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated to obtain 6-methylindane-1-ol (5.5 g). To a solution of 6-methylindane-1-ol in toluene (50 ml) was added p-toluene sulfonic acid monohydrate (0.2 g), and the mixture was stirred for 20 minutes. The temperature of the reaction mixture was returned to room temperature, and the reaction mixture was washed with water, 5% sodium hydrogencarbonate aqueous solution, and saturated saline solution in order and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated to obtain 5-methyl-1H-indene (5.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772407B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-bba1f53cb36c49f8ae1af80aa32433b7 |
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| Source note | uspto-grants-2010_08 |
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