HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 54415333, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Benzoxazol-2-yl)benzyl bromide | HCID 11033515 | — |
| Reactant | HCID 19384402 | HCID 19384402 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54415333 | HCID 54415333 | — |
Reaction Steps
To a mixture of 2-triphenylmethylaminomethyl-1-hydroxymethylcyclopropane (0.338 g; 0.984 mmol) in 30 ml THF and 5 ml DMF is added sodium hydride (60%; 0.059 g; 1.48 mmol) followed by 4-(benzoxazol-2-yl)benzyl bromide (0.255 g; 0.886 mmol) and a pinch of potassium iodide. This is stirred overnight, quenched with water, concentrated in vacuo and flash chromatographed using hexane:ethyl-acetate; 7:1 to obtain trans-2-triphenylmethylaminomethyl-[4-(benzoxazol-2-yl)-benzyloxymethyl]cyclopropane as a pale yellow oil 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-bbf3f3809e4e43489c64016ad1fdf932 |
| Source note | uspto-grants-1995_09 |