HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985713Generated: October 26, 2026
Aniline → 2'-Methylspiro[cyclohexane-1,3'-indole]
https://huagongshe.com/reaction/985713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | 1-Ethynylcyclohexanol | HCID 6525 | — |
| Reactant | Benzenamine hydrochloride (1:1) | HCID 8870 | — |
| Catalyst | Triruthenium dodecacarbonyl | HCID 6096991 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2'-Methylspiro[cyclohexane-1,3'-indole] | HCID 339113 | 1.2% |
Reaction Steps
1-Ethynyl-1-cyclohexanol (1.242 g, 10 mmol), aniline (0.931 g, 10 mmol), Ru3(CO)12 (32.0 mg, 0.05 mmol) and aniline hydrochloride (0.259 g, 2.0 mmol) were placed in a 10 ml round-bottomed flask, and the mixture was stirred at 120° C. for 12 hours. After cooling, dichloromethane (3 mL) was added, and the organic layer was washed twice with 1 M hydrochloric acid (2 mL) and once with water (2 mL). The organic layer was dried over sodium sulfate, and the solvent was distilled away, whereby 2-methyl-3H-indole-3-spiro-1′-cyclohexane (24 mg; 0.12 mmol; yield, 1.2%; purity, 95% or more) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872835B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-5ecff62f5d9440c1ab9b52585fc1ae23 |
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| Source note | uspto-grants-2005_03 |
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