HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyclohexylbenzenamine → Butyl 1-[(4-cyclohexylphenyl)amino]indane-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyclohexylbenzenamine | HCID 80764 | — |
| Reactant | Butyl 1-oxoindane-5-carboxylate | HCID 67484921 | — |
| Reactant | HCID 178419135 | HCID 178419135 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Butyl 1-[(4-cyclohexylphenyl)amino]indane-5-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563815B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-743de3116fac44b1bbd959d38dfdb039 |
| Source note | uspto-grants-2009_07 |