HCID 19810491, compound → 2,2,3,3,4,4-Hexafluorocyclopentanol
Reaction equation
C1([O:7][CH:8]2[CH2:12][C:11]([F:14])([F:13])[C:10]([F:16])([F:15])[C:9]2([F:18])[F:17])CCCCC1>S(=O)(=O)(O)O>[F:17][C:9]1([F:18])[C:10]([F:15])([F:16])[C:11]([F:13])([F:14])[CH2:12][CH:8]1[OH:7]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
276 g (1 mol) of 2,2,3,3,4,4-hexafluorocyclopentyl cyclohexyl ether from Step 2 are added dropwise to 300 ml of concentrated sulphuric acid until the evolution of gas has ceased, and the cleavage product is distilled off at 130°-140° C. The mixture of the desired alcohol and cyclohexene is redistilled. In this manner, distillation gives 2,2,3,3,4,4-hexafluorocyclopentanol.
Workup
- distillationthe cleavage product is distilled off at 130°-140° C
- additionThe mixture of the desired alcohol and cyclohexene
- distillationis redistilled
- distillationIn this manner, distillation
Sources & evidence
- ORD record
- ord-6863689547aa4faaafbcdcbbd68872cc
- Source dataset
- uspto-grants-1992_11
- Patent number
- US05164383
Reaction notes
Loading…