Triethyl phosphonoacetate → HCID 68434177, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[C:11]([O:15][CH3:16])[C:12]=1[O:13][CH3:14])[CH:9]=[C:8]([CH:17]=O)[CH:7]=[CH:6]2.C(OP([CH2:27][C:28]([O:30][CH2:31][CH3:32])=[O:29])(OCC)=O)C>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[C:11]([O:15][CH3:16])[C:12]=1[O:13][CH3:14])[CH:9]=[C:8]([CH:17]=[CH:27][C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH:7]=[CH:6]2Participants
3
Procedure
6,7,8-Trimethoxynaphthalene-2-carboaldehyde (985 mg) and ethyl diethylphosphonoacetate (1.05 mL) were treated in the same manner as in Preparation Example 17 to obtain the title compound.
Sources & evidence
- ORD record
- ord-1f050542efc340c391dd0d067a4dd2c1
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07135473B2
Reaction notes
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