4-Piperidinol, 1,2,2,6,6-pentamethyl- → HCID 67045739, compound
Reaction equation
[CH3:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11].[Cl:13][C:14]1[CH:19]=[CH:18][C:17](O)=[CH:16][C:15]=1[C:21]([F:24])([F:23])[F:22]>>[ClH:13].[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([O:10][CH:5]2[CH2:6][C:7]([CH3:8])([CH3:9])[N:2]([CH3:1])[C:3]([CH3:12])([CH3:11])[CH2:4]2)=[CH:16][C:15]=1[C:21]([F:22])([F:23])[F:24]Participants
3
Procedure
Was prepared according to method A from 1,2,2,6,6-pentamethyl-piperidin-4-ol and 4-chloro-3-trifluoromethylphenol. Mp 240-245° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-74c5d1026f684d8ea7c91319068cb936
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07915419B2
Reaction notes
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