HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → HCID 23111762, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23111825 | HCID 23111825 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23111762 | HCID 23111762 | 99% |
Reaction Steps
3-(1-Benzothiophene-5-yl)benzaldehyde (3.9 g, 16.4 mmol) was dissolved in a mixed solution of ethanol (80 mL) and tetrahydrofuran (20 mL), and the mixture was ice-cooled. Sodium borohydride (0.62 g, 16.4 mmol) was added to the solution. After stirring under ice-cooling for 3 hr, aqueous citric acid solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained oil was crystallized from ethyl acetate-hexane to give the title compound (3.9 g, yield 99%) as colorless prism crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07517910B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-67ff3aab29b8446c927c289de13f624c |
| Source note | uspto-grants-2009_04 |