HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-Methoxyhexan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,6-Hexanediol | HCID 12374 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxyhexan-1-ol | HCID 12651699 | — |
Reaction Steps
Sodium hydride (NaH) (50%, 6.12 g) suspended in tetrahydrofuran (THF) (60 ml) was added to a solution of 1,6-hexanediol (15.0 g) in THF (200 ml), and kept at 60° C. until gas evolution stopped. After cooling, a solution of methyl iodide (12 ml) in THF (35 ml) was added and kept overnight at room temperature. The crude product obtaind after the usual work-up was chromatographed to give 6-methoxy-1-hexanol. Yield; 8.16 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591887 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-95c505f814ea4cd68be433843fa8e854 |
| Source note | uspto-grants-1997_01 |