HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → n-butyl (R)-2-(3-formylphenoxy)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-2-(Trifluoromethylsulfonyloxy)butanoic acid butyl ester | HCID 25023368 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | n-butyl (R)-2-(3-formylphenoxy)butyrate | HCID 11846216 | — |
Reaction Steps
Potassium carbonate (473 mg) was added to a solution of 3-hydroxybenzaldehyde (418 mg) in acetonitrile (10 mL). Subsequently, n-butyl (S)-2-trifluoromethanesulfonyloxybutyrate (1.0 g) was added to the mixture, followed by stirring at room temperature for 12 hours. Ethyl acetate was added to the reaction mixture, and the resultant mixture was washed sequentially with water and saturated brine, followed by drying over sodium sulfate anhydrate. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified through silica gel column chromatography (hexane/ethyl acetate=4/1), to thereby yield 904 mg of a colorless, oily substance (99.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538242B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f3edbdc1d6d14417a7c6af4ca139b6e5 |
| Source note | uspto-grants-2009_05 |