HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457403Generated: October 29, 2026
Hydrochloric Acid → HCID 60123706, compound
https://huagongshe.com/reaction/457403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 20741434 | HCID 20741434 | — |
| Reactant | HCID 178507003 | HCID 178507003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 60123706 | HCID 60123706 | 89% |
Reaction Steps
In an atmosphere of nitrogen, phenylmagnesium bride (3 mol/l diethyl ether solution, 15 ml) was added dropwise to tetrahydrofuran solution (50 ml) of N-methyl-N-methoxy-[1-(R)-phenylethyl]-5-oxopyrrolidine-3-(R)-carboxamide (2.49 g, 9.0 mmol), and the mixture was stirred at room temperature for 30 minutes. The reaction solution was mixed with 1 mol/l hydrochloric acid (50 ml) under ice-cooling and then extracted with ethyl acetate (8 ml×2). The organic layer was washed with saturated brine (100 ml) and then dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure and the resulting residue was applied to a silica gel column chromatography. By eluting with n-hexane:ethyl acetate (1:1), 2.36 g (89%) of the title compound was obtained as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07186843B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-e22c873530b94a3c9600a13f39fbf1c9 |
|---|
| Source note | uspto-grants-2007_03 |
|---|