HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 11032835, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Amino-2-phenylethan-1-ol | HCID 134797 | — |
| Reactant | Methyl 2-[(succinimidooxy)carbonyl]benzoate | HCID 10901878 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11032835 | HCID 11032835 | 40% |
Reaction Steps
To a solution of (S)-2-amino-2-phenylethanol (3 g, 21.87 mmol) in water (26.5 mL), and acetonitrile (46.4 mL) was added 2,5-dioxopyrrolidin-1-yl methyl phthalate (5.76 g, 20.78 mmol) at room temperature. The reaction mixture was stirred at room temperature for overnight. After acetonitrile was removed in vacuo, the reaction mixture was then extracted with EtOAc. The organic was washed by water and brine, dried over anhydrous sodium sulfate, filtered off, and concentrated in vacuo yielding (S)-2-(2-hydroxy-1-phenylethyl)isoindoline-1,3-dione (2.2 g, 40%). LCMS (m/z): 268 (MH+), 0.79 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242996B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-eed24d4ce7e446cc9b2ad05dc5cb950b |
| Source note | uspto-grants-2016_01 |