HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-3-trimethylsilyloxy-azetidine → 1-benzylazetidin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-3-trimethylsilyloxy-azetidine | HCID 3800468 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-benzylazetidin-3-ol | HCID 3801345 | 77.2% |
Reaction Steps
1-Benzyl-3-trimethylsilyloxy-azetidine (1.8 g, 7.65 mmol) prepared in preparation example 25 was dissolved in methanol (9 ml), sodium methoxide (826 mg, 15.29 mmol) was added thereto, and stirred at room temperature for 30 min. The solvent was removed by evaporation under a reduced pressure, and the residue was extracted using ethyl acetate. The organic extract layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated under a reduced pressure, to obtain 0.964 g (yield: 77%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662810B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-99fdf6ae5f874c87a8fd53e869c2f953 |
| Source note | uspto-grants-2010_02 |