HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(1-Amino-propyl)-4-trifluoromethyl-cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Reactant | HCID 67072554 | HCID 67072554 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-(1-Amino-propyl)-4-trifluoromethyl-cyclohexanol | HCID 58380843 | 91.7% |
Reaction Steps
3.22 g (7.26 mmol) of 2-Methyl-propane-2-sulfinic acid {1-[4-(tert-butyl-dimethyl-silanyloxy)-1-trifluoromethyl-cyclohexyl]-propyl}-amide (73) were dissolved using 200 ml of 2-propanol. 60 ml of a 10% aqueous solution of HCl was added and the mixture was stirred for 5 h at ambient temperature and the mixture allowed to stand at ambient temperature for 16 h. Afterwards, 300 ml of a saturated aqueous solution of K2HPO4 were added and the 2-propanol evaporated. The resulting mixture was extracted twice using 100 ml of ethyl acetate each. The organic layer was dried using MgSO4 and evaporated to yield 1.50 g of 74 as an oil, used without further purification. Rt=0.82 min (Method P).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399482B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-051112a5f65a4c10bd18922b09a54ea3 |
| Source note | uspto-grants-2013_03 |