HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 18427235, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1-Bromooctadecane | HCID 8218 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Serinol | HCID 68294 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18427235 | HCID 18427235 | — |
Reaction Steps
A solution of 2-amino-1,3-propanediol in THF is added dropwise with vigorous stirring to a suspension of sodium hydride over a period of 45 minutes to 2 hrs. The reaction mixture is stirred at room temperature for an additional hr and sequentially treated with a solution of one equivalent each of octadecyl bromide and benzyl bromide, respectively. The reaction mixture is stirred at room temperature for 4-14 hrs. The reaction mixture is worked up by extraction with methylene chloride. The methylene chloride layer is washed with water (3×50 mL), saturated NaCl (1×50 mL) and dried (MgSO4). The dried organic layer is evaporated under vacuum to afford the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06379930B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-f012cdd77d3a4454b5da2b56b39c7d00 |
| Source note | uspto-grants-2002_04 |