Diethyl methylphosphonite → HCID 86734184, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1I.[CH2:10]([O:12][P:13]([CH3:17])[O:14]CC)[CH3:11]>[Hg]>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[P:13]([CH3:17])(=[O:14])[O:12][CH2:10][CH3:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Using a high pressure 450 watt mercury lamp, 20 grams of 2,5-dichloroiodobenzene and 30 grams of diethylmethylphosphonite are combined and irradiated for approximately 31/2 hours. After concentration and distillation, a clear oil is obtained, which then solidified. The solid is recrystallized from ethyl ether to give 8.5 g. of white needles having a melting point between 90° and 91° C.
Workup
- customirradiated for approximately 31/2 hours
- concentrationAfter concentration and distillation
- customa clear oil is obtained
- customThe solid is recrystallized from ethyl ether
- customto give 8.5 g
Sources & evidence
- ORD record
- ord-ed614431657e4e09a52b530c0746785e
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03992273
Reaction notes
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