Hydrochloric Acid → HCID 86737289, compound
Reaction equation
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](O)([C:14]([F:17])([F:16])[Cl:15])[C:10]([F:13])([F:12])[Cl:11])=[CH:5][CH:4]=1.[CH3:19][S:20](Cl)(=[O:22])=[O:21].Cl>N1C=CC=CC=1>[CH3:1][N:2]([S:20]([CH3:19])(=[O:22])=[O:21])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]([C:14]([F:17])([F:16])[Cl:15])[C:10]([F:13])([F:12])[Cl:11])=[CH:5][CH:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To 6.1 g (20 mmole) N-methyl-4-(1,3-dichlorotetrafluoro-2-hydroxy-2-propyl)aniline in 30 ml pyridine add 3.4 g (30 mmole) methanesulfonyl chloride. Stir 1.5 hours, pour onto water, acidify with concentrated HCl and filter. Dissolve the solid in 1N NaOH, wash with Et2O, acidify and filter. Recrystallize the solid from Et2O-hexane to give the product; m.p. 140°-142° C.
Workup
- additionpour onto water
- filtrationfilter
- dissolutionDissolve the solid in 1N NaOH
- washwash with Et2O
- filtrationfilter
- customRecrystallize the solid from Et2O-hexane
- customto give the product
Sources & evidence
- ORD record
- ord-344f9741f3604c86a33d3c0f6fd180a4
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04230635
Reaction notes
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