HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphate → (αR)-α-Butyl-2-furanmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Nadh | HCID 439153 | — |
| Reactant | HCID 15701284 | HCID 15701284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (αR)-α-Butyl-2-furanmethanol | HCID 12685003 | — |
Reaction Steps
A reaction mixture was formed by admixing (i) 50 mg NAD, (ii) 4 ml of 2-propanol and (iii) 5 mmoles of butyl 2-furanoyl ketone, Compound 12, in a liquid medium containing 1 gm of lyophilized PED alcohol dehydrogenase preparation, 75 ml of 50 mM phosphate buffer, pH 7.1, and 25 ml of hexane. The pH of the reaction was maintained constant by addition of 1N NaOH. The reaction mixture was maintained at room temperature until product formation stopped. When product formation stopped, (R)-α-butyl-2-furanmethanol, Compound 12a, was isolated by removal of the hexane layer and extraction of the aqueous layer with ethyl ether (3×75 ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05385833 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-5c4548dc2fc34ffea3e060242774dad3 |
| Source note | uspto-grants-1995_01 |