HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 68746626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate | HCID 2734674 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68746626 | HCID 68746626 | 77.8% |
Reaction Steps
Sodium triacetoxyborohydride (15.9 g, 75.4 mmol) and enough acetic acid to bring the pH to 5 were added to a solution of N-tert-butoxycarbonyl-L-prolinal (5 g, 25 mmol) and 4-fluorobenzylamine (6.28 g, 50.3 mmol) in 200 mL of 1,2-dichloroethane. The mixture was stirred at ambient temperature overnight, and then it was diluted with dichloromethane, and washed with saturated sodium bicarbonate solution. The organic phase was dried over magnesium sulfate, filtered and concentrated to leave the crude product. Chromatography (elution with methanol/ethyl acetate) afforded 6.0 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07625889B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-6dfdd5dabb884f2d96abeec53f5a4707 |
| Source note | uspto-grants-2009_12 |