Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | 1-(4-Fluorophenyl)ethylamine | HCID 123063 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14772825 | HCID 14772825 | — |
Reaction Steps
To a solution of racemic 4-fluoro-α-methylbenzenemethanamine (2.95 g, 21.2 mmol) and triethylamine (4.3 mL, 30.9 mmol) in acetonitrile (75 mL) in a flame-dried flask under nitrogen was added dropwise t-butylchlorodiphenylsilane (5.5 mL, 21.1 mmol). The mixture was stirred at room temperature overnight and then filtered to remove the insoluble white precipitate (triethylamine hydrochloride). After removal of the solvent in vacuo, the crude product was taken up in ether and washed sequentially with H2O, saturated NaHCO3 solution and brine. The solution was dried (Na2SO4 /K2CO3) and concentrated to leave a clear oil which was distilled under high vacuum. The major fraction consisting of the pure title compound (3.8 g, 47%) distilled from 123° to 143° C. at 0.15 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05260309 |
|---|
| Source dataset | uspto-grants-1993_11 |
|---|
| ORD ID | ord-a676f5749d134f3099e3b5f79b1a51df |
|---|
| Source note | uspto-grants-1993_11 |
|---|