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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant1-EthynylcyclohexanolHCID 6525—
ReactantBenzenamine hydrochloride (1:1)HCID 8870—
CatalystTriruthenium dodecacarbonylHCID 6096991—
SolventDichloromethaneHCID 6344—
Product2'-Methylspiro[cyclohexane-1,3'-indole]HCID 3391131.2%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872835B2
Source datasetuspto-grants-2005_03
ORD IDord-5ecff62f5d9440c1ab9b52585fc1ae23
Source noteuspto-grants-2005_03