Hydrochloric Acid → HCID 12898548, compound
Reaction equation
[F:1][C:2]([F:19])([F:18])[C:3]([C:9]1[CH:15]=[C:14]([CH3:16])[C:12](N)=[C:11]([CH3:17])[CH:10]=1)([OH:8])[C:4]([F:7])([F:6])[F:5].Cl.N([O-])=O.[Na+].C(OC([S-])=[S:29])C.[K+]>O>[F:1][C:2]([F:19])([F:18])[C:3]([C:9]1[CH:15]=[C:14]([CH3:16])[C:12]([SH:29])=[C:11]([CH3:17])[CH:10]=1)([OH:8])[C:4]([F:7])([F:6])[F:5]Participants
6
Conditions
- Temperature
- 0 °C
Procedure
To 4-(hexafluoro-2-hydroxy-2-propyl)-2,6-dimethylaniline (20.0 g=70 mmol), add 50 ml 4 N HCl. Reflux 1 hr., cool to 0° C., and add over 1 hour NaNO2 (6.0 g=87 mmol) in 13 ml H2O. After 30 min., add to a 45° C. solution of potassium ethylxanthate (14.3 g=83 mmol) in 40 ml H2O. Keep at 45° C. for 30 minutes, cool, and extract with ether. Dry and concentrate. Dissolve the oil in 100 ml EtOH, add potassium hydroxide (17.5 g) and reflux 1 hour. Concentrate, then add 50 ml water and 10 ml concentrated sulfuric acid. Add 0.5 g zinc dust and steam distill. Extract the distillate with ether, dry and concentrate. Recrystallize from hexane to obtain 4-(hexafluoro-2-hydroxy-2-propyl)-2,6-dimethylthiophenol, m.p. 62°-64° C.
Workup
- temperatureReflux 1 hr
- waitKeep at 45° C. for 30 minutes
- temperaturecool
- extractionextract with ether
- customDry
- concentrationconcentrate
- dissolutionDissolve the oil in 100 ml EtOH
- additionadd potassium hydroxide (17.5 g)
- temperaturereflux 1 hour
- concentrationConcentrate
- additionadd 50 ml water and 10 ml concentrated sulfuric acid
- additionAdd 0.5 g zinc dust and steam
- distillationdistill
- extractionExtract the distillate with ether
- customdry
- concentrationconcentrate
- customRecrystallize from hexane
Sources & evidence
- ORD record
- ord-532149e97cf649478396a44e4baf4802
- Source dataset
- uspto-grants-1981_06
- Patent number
- US04272550
Reaction notes
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