HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-((Tert-butyldiphenylsilyl)oxy)azetidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | 3-Hydroxyazetidine hydrochloride | HCID 2759290 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-((Tert-butyldiphenylsilyl)oxy)azetidine | HCID 17842531 | 82.5% |
Reaction Steps
To a solution of azetidin-3-ol hydrochloride (5.11 g, 46.7 mmol, 1.0 equiv) and 1H-imidazole (9.52 g, 140 mmol, 3.0 equiv) in DCM (100 mL) at 0° C. was added TBDPSCl (19.18 g, 70 mmol, 1.5 equiv) dropwise. The resulting mixture was stirred at rt overnight and then diluted with water, and extracted with DCM. The combined organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The crude product was eluted over a silica gel with DCM/MeOH=1001 to 101 to give 12 g of 3-(tert-butyldiphenylsilyloxy)azetidine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266895B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-0652ca58e7f94ef0a03f0f98ec0ba0d0 |
| Source note | uspto-grants-2016_02 |