HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-5-benzyloxymethyl-2,2-diphenylmorpholine-4-carboxylic acid tert-butyl ester → (R)-5-Formyl-2,2-diphenylmorpholine-4-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-5-benzyloxymethyl-2,2-diphenylmorpholine-4-carboxylic acid tert-butyl ester | HCID 68561079 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-5-Formyl-2,2-diphenylmorpholine-4-carboxylic acid tert-butyl ester | HCID 86615365 | — |
Reaction Steps
To 10% palladium on carbon (2.1 g) in ethanol (50 mL) add (S)-5-benzyloxymethyl-2,2-diphenylmorpholine-4-carboxylic acid tert-butyl ester (3.29 g, 7.16 mmol) in ethanol (75 mL) and stir under 1 atmosphere of hydrogen gas at room temperature for 4 hours. Filter and concentrate to give the desired compound as a white solid. Dissolve the solid in dimethylsulfoxide (20 mL) and add triethylamine (1.30 g, 12.82 mmol), then pyridine sulfur trioxide complex (1.84 g, 11.55 mmol). Stir at room temperature 3 hours and dilute with 10% ethyl acetate/hexanes (˜150 mL). Wash with water, 1 N aqueous citric acid and saturated aqueous sodium chloride, dry (magnesium sulfate), filter and concentrate to give the desired compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745438B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-dff332a6a8d240d9bc709087f7d05a66 |
| Source note | uspto-grants-2010_06 |