Trimethyl phosphite → HCID 21612902, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:14])[CH:5]([NH:11][CH:12]=[O:13])[CH:6](O)[C:7]([CH3:9])=[CH2:8])[CH3:2].S(Br)(Br)=O.[P:19]([O:24]C)([O:22][CH3:23])[O:20][CH3:21]>>[CH2:1]([O:3][C:4](=[O:14])[CH:5]([NH:11][CH:12]=[O:13])/[CH:6]=[C:7](\[CH3:9])/[CH2:8][P:19]([O:22][CH3:23])([O:20][CH3:21])=[O:24])[CH3:2]Participants
4
Procedure
By reaction of 2-formylamino-3-hydroxy-4-methyl-4-pentenoic acid ethyl ester with thionyl bromide and subsequent treatment with trimethyl phosphite in a manner analogous to that described in Example 1, E-2-formylamino-4-methyl-5-dimethylphosphono-3-pentenoic acid ethyl ester is obtained in the form of a pale yellow oil.
Sources & evidence
- ORD record
- ord-84dc490d9fe241eaa6515d0195deb6b7
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05051413
Reaction notes
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