HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → [4-Hydroxy-3'-(hydroxymethyl)-6-methylbiphenyl-2-yl]methyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (4-Acetoxy-3'-formyl-6-methylbiphenyl-2-yl)methyl acetate | HCID 59342569 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [4-Hydroxy-3'-(hydroxymethyl)-6-methylbiphenyl-2-yl]methyl acetate | HCID 59342611 | 71.4% |
Reaction Steps
To a solution of (4-acetoxy-3′-formyl-6-methylbiphenyl-2-yl)methyl acetate (1.63 g, 4.99 mmol) in a mixed solvent of tetrahydrofuran (10 mL) and methanol (5 mL) was added sodium borohydride (90%, 0.210 g, 5.00 mmol) under ice-cooling, and the mixture was stirred at the same temperature for 3 hr under nitrogen atmosphere. Aqueous citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=20:80-80:20) to give the title compound (1.02 g, yield 71%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088821B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-ded71389e8174b06a9049b53f4ee9a69 |
| Source note | uspto-grants-2012_01 |