3',5'-Dichloro-2'-hydroxyacetophenone → 2,4-Dichloro-6-(1'-hydroxyethyl)phenol
Reaction equation
[CH3:1][C:2]([C:4]1[C:9]([OH:10])=[C:8]([Cl:11])[CH:7]=[C:6]([Cl:12])[CH:5]=1)=[O:3].[BH4-].[Na+]>C(O)C>[Cl:11][C:8]1[CH:7]=[C:6]([Cl:12])[CH:5]=[C:4]([CH:2]([OH:3])[CH3:1])[C:9]=1[OH:10]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3,5-Dichloro-2-hydroxyacetophenone (40 g) was treated in ethanol with sodium borohydride (4 g). The solid reaction product was recrystallized from benzene to give 2,4-dichloro-6-(1'-hydroxy ethyl) phenol (32 g, m.p. 70°).
Workup
- customThe solid reaction product
- customwas recrystallized from benzene
Sources & evidence
- ORD record
- ord-d39073fcbf1340ba818bad721d4826bf
- Source dataset
- uspto-grants-1979_08
- Patent number
- US04163801
Reaction notes
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