HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-4-chlorobutane → 1,2-bis[N-(4-chlorobutyl)-N-propionylamino]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | N-[2-(propanoylamino)phenyl]propanamide | HCID 694922 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1,2-bis[N-(4-chlorobutyl)-N-propionylamino]benzene | HCID 19079254 | 12.6% |
Reaction Steps
To a suspension of 3.27 g (15 mmol) of 1,2-dipropionylaminobenzene, 4.32 ml (37.5 mmol) of 4-bromo-1-chlorobutane, and 0.96 g (3.0 mmol) of tetrabutylammonium bromide in 25 ml of toluene, 5.6 ml of 50% aqueous sodium hydroxide was added at room temperature, and the mixture was stirred for 16 hours. The organic layer was separated, washed with saturated aqueous sodium chloride, and dried. The solvent was distilled off and the residue was purified by column chromatography (eluent:hexane/ethyl acetate=2:1 to 1:1 to 1:2 to 1:4) to give 0.76 g of the desired product (12.6% yield, white crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561147 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-a316a22cb8d949b5842ab7e316b0ef88 |
| Source note | uspto-grants-1996_10 |