HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorine → p-Nitrobenzyl 2-(4-chloro-2-oxo-1-azetidinyl)-4,4-dimethyl-3-oxopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | p-Nitrobenzyl 2-(4-tert-butylthio-2-oxo-1-azetidinyl)-4,4-dimethyl-3-oxopentanoate | HCID 14460290 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-Nitrobenzyl 2-(4-chloro-2-oxo-1-azetidinyl)-4,4-dimethyl-3-oxopentanoate | HCID 14460330 | 90.9% |
Reaction Conditions
| Temperature | -50 °C |
|---|
Reaction Steps
A solution of 439 mg (1.0 mmol) of p-nitrobenzyl 2-(4-tert-butylthio-2-oxo-1-azetidinyl)-4,4-dimethyl-3-oxopentanoate in 20 ml of dry methylene chloride is cooled to -50° C. and a solution of 166 mg of chlorine in 1.6 ml of carbon tetrachloride is added. After stirring for 30 minutes at -50° C., the solvent is evaporated in vacuo and the residue is recrystallized from methylene chloride/hexane, the product (348 mg) being obtained as a crystalline solid as a 6:4 mixture of the two diastereomeric title compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05108747 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-aed38769fca24f7aafd6a3e1e02050d9 |
| Source note | uspto-grants-1992_04 |