HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67303368, compound → HCID 67303639, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67303368 | HCID 67303368 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67303639 | HCID 67303639 | 56.8% |
Reaction Steps
A solution of benzyl 2-(adamantan-2-yl)-3-oxo-1,2-diazetidine-1-carboxylate (100 mg, 0.29 mmol) in tetrahydrofuran (5 mL) was added with 10% palladium carbon (catalyst amount), and under a hydrogen atmosphere, the resultant was stirred at room temperature for 10 hours. The reaction solution was filtered using celite, concentrated in vacuo, and the obtained residue was purified using silica gel chromatography (hexane:ethyl acetate=1:1), and 2-(adamantan-2-yl)-1,2-diazetidin-3-one (34.0 mg, 56.8%) 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-d858d42aa9594c8d9202fbfea3367192 |
| Source note | uspto-grants-2012_08 |