HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 178453937, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2-Methylpentane | HCID 7892 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178453955 | HCID 178453955 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178453937 | HCID 178453937 | — |
Reaction Steps
Trans-(4-Formyl-cyclohexyl)carbamic acid tert-butyl ester (3.27 g, 14.38 mmol) and aniline (1.98 mL, 15.81 mmol) are dissolved in dichloromethane (60 mL) at room temperature. Sodium triacetoxyborohydride (4.57 g, 21.57 mmol) is added in one portion and the mixture is stirred at room temperature for 2.5 hours. 1N sodium hydroxide solution (20 mL) is added and the mixture is stirred at room temperature for a further 10 minutes. The DCM layer is separated and washed successively with water and saturated brine, dried (MgSO4), filtered and evaporated to give a colourless solid. This is slurried with iso-hexane, filtered and dried to give a colourless solid; [MH+ 305]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273900B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-1afc0f155e3d4b5a96eab3b203346af3 |
| Source note | uspto-grants-2012_09 |