Sodium borohydride → HCID 21405704, compound
Reaction equation
[BH4-].[Na+].C([O:6][C:7]1[CH:12]=[CH:11][C:10]([N:13]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:16](=[O:23])[CH2:15][CH2:14]2)=[CH:9][CH:8]=1)(=O)C>>[OH:6][C:7]1[CH:8]=[CH:9][C:10]([N:13]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[CH:16]([OH:23])[CH2:15][CH2:14]2)=[CH:11][CH:12]=1Participants
3
Procedure
Conventional sodium borohydride reduction of compound A [method see Example 2c), below] yields 1-p-hydroxyphenyl-4-hydroxy-1,2,3,4-tetrahydro-quinoline.
Sources & evidence
- ORD record
- ord-e14b2fcbd42c4fc9838d5808c4d6a79a
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03992386
Reaction notes
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