HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → tert-Butyl [(5-methyl-1,3,4-oxadiazol-2-yl)methyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | Carbonylimidazole | HCID 13571086 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl [(5-methyl-1,3,4-oxadiazol-2-yl)methyl]carbamate | HCID 57366760 | 107.9% |
Reaction Steps
To a stirred solution of Boc-Glycine (1.75 g, 10.0 mmol) in CH2Cl2 at 0° C. was added carbonyl imidazole (1.7 g, 10.5 mmol) and the reaction was stirred for 30 min and then acetic hydrazide (740 mg, 10.0 mmol) was added. After 45 min, CBr4 (6.63 g, 20.0 mmol) and PPh3 (5.25 g, 20.0 mmol) were added and the reaction was stirred overnight at room temperature. The reaction mixture was concentrated partially and chromatographed (50% EtOAc in hexanes) to provide 2.3 g of tert-butyl (5-methyl-1,3,4-oxadiazol-2-yl)methylcarbamate with some triphenylphosphine oxide as impurity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299267B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-d0362ba986db4ab38717d9d120190627 |
| Source note | uspto-grants-2012_10 |