HCID 66930885, compound → HCID 66931163, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]=[CH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>[Pd].CCOC(C)=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
1-(2-Methoxyphenyl)-7-phenoxy-heptane (8.3) was synthesized as described in 8.1 using 7.3 (0.35 g, 1.18 mmol), AcOEt (20 mL), and 10% Pd/C (0.050 g, 14% w/w). The title compound (8.3) was isolated as a colorless viscous liquid (0.33 g, 95% yield).
Workup
- custom1-(2-Methoxyphenyl)-7-phenoxy-heptane (8.3) was synthesized
Sources & evidence
- ORD record
- ord-2bbe4c9a38864084b851d878e5199f6c
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102622B2
Reaction notes
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