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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230024Generated: October 27, 2026

4-Cyclohexylbenzenamine → Butyl 1-[(4-cyclohexylphenyl)amino]indane-5-carboxylate

https://huagongshe.com/reaction/230024

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyclohexylbenzenamineHCID 80764—
ReactantButyl 1-oxoindane-5-carboxylateHCID 67484921—
ReactantHCID 178419135HCID 178419135—
SolventMethanolHCID 887—
ProductButyl 1-[(4-cyclohexylphenyl)amino]indane-5-carboxylateHCID 57586900—

Reaction Steps

To a solution of butyl 1-oxoindane-5-carboxylate (2.0 g, 8.60 mmol) and 4-cyclohexylaniline (2.28 g, 20.64 mmol) in 30 mL of anhydrous MeOH was added decaborane B10H14 (0.32 g, 2.6 mmol) at room temperature under nitrogen. The resulting solution was stirred at room temperature for 1648 h. Product butyl 1-[(4-cyclohexylphenyl)amino]indane-5-carboxylate was collected by filtration as a white solid. HPLC/MS: m/z=392.3 (M+1), Rt=4.97 min. 1H NMR (CDCl3): δ 7.80 (1H, s), 7.97 (1H, d, J=8.0 Hz), 7.48 (1H, d, J=8.0 Hz), 7.14 (2H, d, J=8.5 Hz), 6.74 (2H, d, J=8.5 Hz), 5.07 (1H, t, J=7.1 Hz), 4.39 (2H, t, J=6.7 Hz), 3.92 (1H, br s), 3.10 (1H, m), 2.97 (1H, m), 2.69 (1H, m), 2.49 (1H, m), 2.02-1.80 (8H, m), 1.60-1.31 (7H, m), 1.08 (3H, t, J=7.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563815B2
Source datasetuspto-grants-2009_07
ORD IDord-743de3116fac44b1bbd959d38dfdb039
Source noteuspto-grants-2009_07