HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → cis-2-Triphenylmethylaminocyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1R,2S)-2-aminocyclohexan-1-ol hydrochloride | HCID 12228413 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cis-2-Triphenylmethylaminocyclohexanol | HCID 54233547 | — |
Reaction Steps
A mixture of cis-2-aminocyclohexanol hydrochloride (4.88 g; 32 mmol) (William S. Johnson and Elliot N. Schubert, J.A.C.S., Vol. 72, pp. 2187-2190 (1950), triphenylmethylchloride (10.7 g; 38.4 mmol) and triethylamine (16 ml; 115 mmol) in 250 ml methylene chloride are refluxed for 3 hrs. then stirred at room temperature overnight. The mixture is poured into H2O and extracted with CH2Cl2 (200 ml), dried (Na2SO4) concentrated in vacuo and flash chromatographed using 9:1 7:1; hexane:EtOAc to obtain cis-2-triphenylmethylaminocyclohexanol which is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05451596 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-76b8b4c2cdec433c9a174a2e1b9b67bd |
| Source note | uspto-grants-1995_09 |