HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanediol → HCID 22174480, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | HCID 9965373 | HCID 9965373 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22174480 | HCID 22174480 | — |
Reaction Steps
The reaction and work up was conducted as described in the preparation of compound 415. Starting materials were NaH (60% in oil, 0.86 g, 22 mmol) in THF (80 mL), 1,3-propanediol (8.67 mL, 120 mmol), 2-bromobenzylbromide (5.0 g, 20 mmol) dissolved in 4 mL dry THF and tetrabutylammonium iodide (0.07 g, 0.2 mmol). The crude product was purified by flash chromatography using EtOAc/petroleum ether 1:1->2:1 as the eluent to afford the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07034015B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-ff92c76aa6c549528883310b9552f661 |
| Source note | uspto-grants-2006_04 |