HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 53682744, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,3,4,5,6,7-Hexahydro-2-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[3,4-c]pyridine | HCID 19908254 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53682744 | HCID 53682744 | 85% |
Reaction Steps
1.8 g of N8 -(p-toluenesulfonyl)-3,8-diazabicyclo[4.3.0]non-1(6)-ene, prepared in preparation 8, was dissolved in 30 ml of methanol. 6 ml of 50% aqueous sodium hydroxide solution and 1.5 ml of benzyl bromide were added to the solution and stirred at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure to remove methanol and then extracted with methylene chloride (30 ml×3). It was dried (Na2SO4) and concentrated and then dried under reduced pressure. 2 g of the title compound was obtained (yield 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05091384 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-1d44a7817b5843e890055204f6a842e8 |
| Source note | uspto-grants-1992_02 |