Sodium Hydroxide → HCID 23445637, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:7][C:6]([CH:15]=[O:16])=[CH:5][C:4]=1[CH3:17].[OH-:18].[Na+]>[Ag-]=O>[CH3:1][O:2][C:3]1[C:8]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:7][C:6]([C:15]([OH:18])=[O:16])=[CH:5][C:4]=1[CH3:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared according to the procedure in Example 6, step 3 using 6-methoxy-5-methyl-biphenyl-3-carbaldehyde (1.53 g, 6.77 mmol), silver (I) oxide (1.56 g, 6.77 mmol) and NaOH (2.71 g, 67.7 mmol) to give 1.46 g (89%) of the title compound as a white solid, mp 165-168° C. 1H NMR (DMSO-d6) 6 2.34 (s, 3H), 3.36 (s, 3H), 7.38-7.55 (m, 5H), 7.71 (d, 1H), 7.81 (dd, 1H). IR (KBr) 3400, 2950, 1700, 1600 and 1410 cm−1. mass spectrum (EI), m/z 242 (M+). Anal. Calcd. for C15H14O3.0.2 H2O: C, 73.27; H, 5.91; N, 0.00. Found: C, 73.21; H, 5.93; N, 0.17.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-046495c013f3440e935040308e9e7a20
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248764B1
Reaction notes
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