Methanol → HCID 23465074, compound
Reaction equation
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[C:13]([C:14](Cl)=[O:15])=[CH:12][S:11][N:10]=2)[CH:4]=1.[CH3:19][OH:20]>>[F:1][C:2]([F:18])([F:17])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[C:13]([C:14]([O:20][CH3:19])=[O:15])=[CH:12][S:11][N:10]=2)[CH:4]=1Participants
3
Procedure
A solution of 2.92 g (0.010 mol) of 3-(α, α, α-trifluoro-m-tolyl)-4-isothiazolecarbonyl chloride prepared as in Example 29 and 10 ml of methanol was held at reflux for 0.5 hours and was concentrated under vacuum to 80° (0.3 torr) to 2.72 g of oil, nD23.4° = 1.5404.
Workup
- temperatureat reflux for 0.5 hours
- concentrationwas concentrated under vacuum to 80° (0.3 torr) to 2.72 g of oil, nD23
- custom4° = 1.5404
Sources & evidence
- ORD record
- ord-aa1babe661554af89812252d3fc8bdc4
- Source dataset
- uspto-grants-1979_03
- Patent number
- US04144047
Reaction notes
Loading…