HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 54116443, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2H-Pyran, tetrahydro-2-[(3-methyl-3-butenyl)oxy]- | HCID 12290655 | — |
| Catalyst | Mercury | HCID 23931 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 54116443 | HCID 54116443 | 93% |
Reaction Steps
To 2-(3-methyl-3-butenyloxy)tetrahydropyran (150.0 g, 881.0 mmol) in methanol (600 ml) was added mercuric acetate (309 g, 969 mmol) and the mixture was stirred until it became homogeneous. To this solution was added 0.5N NaOH (500 ml) in one portion followed by dropwise addition of 0.5N NaBH4 in 0.5N NaOH (500 ml). The mixture is stirred until mercury metal congeals at the bottom of the flask. The solution is decanted into a separatory funnel and extracted with ether (3×300 ml). The combined ethereal extracts are dried (MgSO4) and concentrated to afford 166 g (93%) of 2-(3-methoxy-3-methylbutyloxy)tetrahydropyran as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112595 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-0db9edb1f4f04f4ab51c23f8f722f250 |
| Source note | uspto-grants-1992_05 |