Hydrochloric Acid → HCID 86756307, compound
Reaction equation
C[CH:2]1[CH2:6][S:5][CH:4]([C:7]([O:9][CH:10]([CH3:12])[CH3:11])=[O:8])[C:3]1=[N:13][OH:14].[ClH:15]>C(OC)(C)(C)C>[Cl:15][CH:2]1[CH2:6][S:5][CH:4]([C:7]([O:9][CH:10]([CH3:12])[CH3:11])=[O:8])[C:3]1=[N:13][OH:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
334 g (1.54 mol) of i-propyl 4-methyl-3-hydroximino-tetrahydrothiophene-2-carboxylate are dissolved in 5 litres of methyl tert-butyl ether and cooled using an ice bath. Hydrogen chloride is then—after the ice bath had been removed—introduced with stirring for two hours. The mixture is subsequently concentrated using water pump vacuum and the amorphous residue is crystallized from acetone.
Workup
- temperaturecooled
- additionhad been removed—introduced
- concentrationThe mixture is subsequently concentrated
- customthe amorphous residue is crystallized from acetone
Sources & evidence
- ORD record
- ord-0c86c81b47024bada760e5b2fd019c85
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06180567B2
Reaction notes
Loading…