HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 2-Methanesulfinylmethyl-3-methoxy-benzoic acid n'-tert-butyl-n'-(3,5-dimethyl-benzoyl)-hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-Methoxy-2-methylsulfanylmethyl-benzoic acid n'-tert-butyl-n'-(3,5-dimethyl-benzoyl)-hydrazide | HCID 59838589 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methanesulfinylmethyl-3-methoxy-benzoic acid n'-tert-butyl-n'-(3,5-dimethyl-benzoyl)-hydrazide | HCID 59838601 | — |
Reaction Steps
3-Methoxy-2-methylsulfanylmethyl-benzoic acid N′-tert-butyl-N′-(3,5-dimethyl-benzoyl)-hydrazide in CH2Cl2 was stirred at room temperature with 1.0 eq of m-chloroperbenzoic acid. The reaction was complete within 5 min as indicated by TLC. The reaction mixture was washed with saturated NaHCO3 and the organic layer was stripped under vacuum. The residue was mixed with 1-2 mL of 1:1 ether:hexane and the solution was removed with a pipette, leaving the product which was then dried under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563928B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-4fdd7b096ab64284a32bc098836cf19a |
| Source note | uspto-grants-2009_07 |