HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 3-(Benzylamino)-1,1,1-trifluoropropan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-(Trifluoromethyl)oxirane | HCID 520769 | — |
| Reactant | Trifluoromethanesulfonic acid, lithium salt | HCID 3664839 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(Benzylamino)-1,1,1-trifluoropropan-2-ol | HCID 3787794 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
Lithium triflate was suspended in CH3CN (15 mL) and the mixture is cooled to −10° C. 2-(Trifluoromethyl)oxirane is added and the suspension is allowed to warm to RT with stirring. Benzylamine (6.33 mL, 58 mmol, Aldrich) is added all-at-once and the resultant solution is stirred for 25 minutes. The reaction is quenched by pouring into CH2Cl2 (200 mL) and washing 3× with H2O (200 mL). The organic layer is dried over Na2SO4 and filtered. The product is purified on a Biotage Flash 75L using 20:70:10 CH2Cl2:pentane:triethylamine as eluent. The product containing fractions are pooled and the solvent is removed by rotary evaporation. The product is dried under vacuum at 100° C. yielding a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605157B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-087e9a7eb0cb46e1883054e14dfd2956 |
| Source note | uspto-grants-2009_10 |