Hydrogen Peroxide → HCID 22765156, compound
Reaction equation
[Cl:1][CH2:2][CH2:3][S:4]([CH2:7][CH2:8][C:9]([NH:11][CH2:12][CH2:13][S:14][CH:15]=[CH2:16])=[O:10])(=[O:6])=[O:5].[OH:17]O>C(O)(=O)C>[Cl:1][CH2:2][CH2:3][S:4]([CH2:7][CH2:8][C:9]([NH:11][CH2:12][CH2:13][S:14]([CH:15]=[CH2:16])=[O:17])=[O:10])(=[O:5])=[O:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 6 g Intermediate 2 in 25 ml acetic acid was treated at 20° C. with 2.5 ml of 30 % hydrogen peroxide and 3 ml acetic acid. After 2 hours the solution was evaporated and the residue stirred with ether. The solid was filtered, dried and recrystallised from ethanol-petrolether. Yield 4.85 g; Mp. 108° to 109° C.
Workup
- customAfter 2 hours the solution was evaporated
- filtrationThe solid was filtered
- customdried
- customrecrystallised from ethanol-petrolether
Sources & evidence
- ORD record
- ord-e459a77a6f2043d4b7b9f1eb0f6bbedb
- Source dataset
- uspto-grants-1978_10
- Patent number
- US04120898
Reaction notes
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