HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 1-Benzyloxy-3-hexadecyloxy-2-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Hexadecyloxybutane-1,2-diol | HCID 14233161 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyloxy-3-hexadecyloxy-2-butanol | HCID 15052293 | 19.3% |
Reaction Steps
In 100 ml of dry dimethylformamide, 17.67 g of 3-hexadecyloxybutane-1,2-diol was treated with 2.36 g of 60% sodium hydride under chilling with ice. To the chilled mixture was added 6.77 g of benzyl chloride, and the resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was recovered in a conventional manner and purified by silica gel column chromatography to give 4.33 g of 1-benzyloxy-3-hexadecyloxy-2-butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05183811 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-9ccfcdb4c22d4fba9b2797ab4f2f7125 |
| Source note | uspto-grants-1993_02 |