HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzylamine → 1-Acetoxy-4-dibenzylamino-2-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | 2-Butene-1,4-diol diacetate | HCID 140402 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Acetoxy-4-dibenzylamino-2-butene | HCID 53789779 | — |
Reaction Steps
A solution of dibenzylamine (40 g, 0.2 mol) and 2-butene-1,4-diol diacetate (105 g, 0.61 mol) dissolved in 150 ml of tetrahydrofuran (THF) is treated with tetrakis(triphenylphosphine)palladium (0) (1.0 g, 0.9 mmol) and stirred at room temperature overnight. The reaction mixture is concentrated in vacuo and the excess 2-butene-1,4-diol diacetate is removed by bulb-to-bulb distillation at 80°-90° C./1 mm. The residue is purified by eluting through a short plug of silica gel (1:1 ethyl acetate:hexanes). 1-Acetoxy-4-dibenzylamino-2-butene is obtained in a yield of 59.2 g (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05283367 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-0039da619408433a8d07dc38e5d0ec31 |
| Source note | uspto-grants-1994_02 |