Naphthalene → 2-Naphthol
Reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.C1([OH:21])C2C(=CC=CC=2)C=CC=1>>[CH:9]1[C:10]2[C:5](=[CH:4][CH:3]=[CH:2][CH:1]=2)[CH:6]=[CH:7][C:8]=1[OH:21]Participants
3
Reactant 2
Product 1
Procedure
A further selective hydroxylation reaction was carried out with the sol-gel-embedded CYP BM-3 on the substrate naphthalene. 77% of the precursor were hydroxylated. The main product obtained was 1-naphthol (85%), and 2-naphthol was obtained as by-product (15%) (detected by gas chromatography).
Workup
- customA further selective hydroxylation reaction
- customThe main product obtained
Sources & evidence
- ORD record
- ord-ce55d738f0c848d28cf32b3480e4ec81
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07364884B2
Reaction notes
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