HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-nitrobenzyl 2-diazo-4-[(2R, 3S)-3-(1-methoxy-1-methylethyl)-4-oxo-azetidin-2-yl]-3-oxobutanoate → 4-nitrobenzyl (2R, 5R, 6S)-3,7-dioxo-6-(1-methoxy-1-methylethyl)-1-azabicyclo[3.2.0]-heptane-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-nitrobenzyl 2-diazo-4-[(2R, 3S)-3-(1-methoxy-1-methylethyl)-4-oxo-azetidin-2-yl]-3-oxobutanoate | HCID 86741280 | — |
| Catalyst | Acetic acid, rhodium(2+) salt | HCID 21674 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-nitrobenzyl (2R, 5R, 6S)-3,7-dioxo-6-(1-methoxy-1-methylethyl)-1-azabicyclo[3.2.0]-heptane-2-carboxylate | HCID 86741282 | 95.1% |
Reaction Steps
A mixture of 4-nitrobenzyl 2-diazo-4-[(2R, 3S)-3-(1-methoxy-1-methylethyl)-4-oxo-azetidin-2-yl]-3-oxobutanoate (56.5 mg) and a catalytic amount of rhodium (II) acetate (ca. 1 mg) in dry benzene (5.6 ml) was refluxed for 30 minutes. After cooling to ambient temperature, the mixture was filtered and evaporated in vacuo to give 4-nitrobenzyl (2R, 5R, 6S)-3,7-dioxo-6-(1-methoxy-1-methylethyl)-1-azabicyclo[3.2.0]-heptane-2-carboxylate (50.0 mg) as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04640915 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-1b6d123353e2415484d5eb6094393a88 |
| Source note | uspto-grants-1987_02 |