HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 67303368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 67303134 | HCID 67303134 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67303368 | HCID 67303368 | 70.5% |
Reaction Steps
Under an argon atmosphere, a solution of benzyl 2-(2-chloroacetyl)-2-(adamantan-2-yl)hydrazinecarboxylate (726 mg, 1.93 mmol) in tetrahydrofuran (20 mL) was added at 0° C. with potassium-t-butoxide (238 mg, 2.12 mmol), and the resultant was stirred at the same temperature for 1 hour. The reaction solution was added with a saturated aqueous solution of ammonium chloride, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, the obtained residue was purified using silica gel chromatography (hexane:ethyl acetate=3:1), and benzyl 2-(adamantan-2-yl)-3-oxo-1,2-diazetidine-1-carboxylate (463 mg, 70.4%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08252781B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-e7a44247ce474c228b534e448347a5c0 |
| Source note | uspto-grants-2012_08 |