HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)benzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)benzaldehyde | HCID 21474525 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)benzenemethanol | HCID 21474532 | — |
Reaction Steps
1.6 g (5 mmol) of the aldehyde obtained in Example 45, 50 ml of THF and 50 ml of methanol are introduced into a round-bottomed flask. 100 mg (2.5 mmol) of sodium borohydride are added in small portions and the mixture is stirred at room temperature for 4 h. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567721 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-c31ca946f76b460aa616114b3d2b0c6d |
| Source note | uspto-grants-1996_10 |