HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (3-Hexyl4-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 3-hexyl-4-methoxybenzoate | HCID 19363353 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Hexyl4-methoxyphenyl)methanol | HCID 19363218 | — |
Reaction Steps
Methyl 3-hexyl-4-methoxybenzoate (93.2 mg, 0.372 mmol) and THF (2 ml) were mixed in a stream of argon. To this solution was added LAH (19 mg, 0.5 mmol) under ice-cooling, and the mixture was stirred for 1 hour. To this reaction mixture were successively added dropwise water (0.019 ml), a 1N aqueous sodium hydroxide solution (0.019 ml) and water (0.06 ml). Ether (20 ml) was added, and the mixture was vigorously stirred for 1 hour. The inorganic salt was filtered off, and the filtrate was concentrated under reduced pressure to give a crude product of (3-hexyl4-methoxyphenyl)methanol. The obtained product was not further purified, and used in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06017919 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-48908c63ce3f42d4bf358c2de6520038 |
| Source note | uspto-grants-2000_01 |