HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (3R,4S)-4-Phenyl-3-[(triethylsilyl)oxy]azetidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Chlorotriethylsilane | HCID 13819 | — |
| Reactant | 2-Azetidinone | HCID 136721 | — |
| Product | (3R,4S)-4-Phenyl-3-[(triethylsilyl)oxy]azetidin-2-one | HCID 10826417 | — |
Reaction Steps
To azetidinone LXXI (580 mg, 3.55 mmol) in dry THF (5.0 mL) was added imidazole (265.5 mg, 3.90 mmol), followed by triethylsilyl chloride (TESCl, 0.654 mL, 3.90 mmol). The mixture was allowed to be stirred for 1 h. Ethyl acetate was added and the organic layer was washed with brine, 10% aqueous HCl and dried. Silica gel chromatography (being eluted with 25% ethyl acetate in hexane) gave 670 mg (Y: 68%) of compound LXXII as a foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05272171 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-f4989d7c15c64ddf8f0593550af48222 |
| Source note | uspto-grants-1993_12 |