HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10173067, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,N-Diethylethanamine trihydrofluoride | HCID 175505 | — |
| Reactant | HCID 59645174 | HCID 59645174 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10173067 | HCID 10173067 | 50.3% |
Reaction Steps
To a solution of the compound from Step J (230 mg, 0.44 mmol) in anhydrous THF (5 mL), was added triethylamine (300 μL, 2.14 mmol) and triethylamine trihydrofluoride (750 μL, 4.5 mmol). The solution was stirred overnight at room temperature. The reaction mixture was then diluted with ethyl acetate (30 mL) and washed with saturated aqueous sodium bicarbonate (3×10 mL) and water (10 mL). After drying the organic layer over anhydrous sodium sulfate and filtration, the solvent was evaporated. The resulting oil was purified on a silica gel column eluting with 1:1 acetone/CH2Cl2 followed by 10% MeOH in CH2Cl2. The appropriate fractions were concentrated and lyophilized to afford the title compound as a colorless powder (90 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07323453B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-be38c2c4707a40dda26195b0571af317 |
| Source note | uspto-grants-2008_01 |