Trimethyl phosphite → Phosphinecarboxylic acid, dimethoxy-, butyl ester, oxide
Reaction equation
C[O:2][P:3]([O:6][CH3:7])[O:4][CH3:5].Cl[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH3:15])=[O:10]>>[CH2:12]([O:11][C:9]([P:3](=[O:2])([O:6][CH3:7])[O:4][CH3:5])=[O:10])[CH2:13][CH2:14][CH3:15]Participants
3
Procedure
From 10.0 ml (85 mmole) of trimethylphosphite and 8.7 g (64 mmole) of n-butyl chloroformate. (100° C., 1.5 hours). Yield 10.9 g (81%). Bp1.0 97°-100° C. nD25 1,4269.
Workup
- custom(100° C., 1.5 hours)
- customBp1.0 97°-100° C.
Sources & evidence
- ORD record
- ord-ba4cc6d1032a4712a11df0aa739d8dbf
- Source dataset
- uspto-grants-1983_05
- Patent number
- US04386081
Reaction notes
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