Methane → HCID 53939749, compound
Reaction equation
[O:1]=[C:2](Cl)OC(Cl)(Cl)Cl.[NH2:9][CH:10]([CH2:15][CH:16]=[CH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:11]([O:13][CH3:14])=[O:12].C>O1CCOCC1>[N:9]([CH:10]([CH2:15][CH:16]=[CH:17][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)[C:11]([O:13][CH3:14])=[O:12])=[C:2]=[O:1]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
0.35 mol diphosgene is added dropwise over 1 hour to a mixture of 0.28 mol of methyl 2-amino-5-phenyl-4-pentenoate, prepared as described by D. Ferroud, J. P. Gene:, and R. Kiolle in Tetrahedron Letters, 1986, 27, 23-26, and 0.4 g activated charcoal in 400 mL dioxane under N2. The reaction mixture is then heated and stirred at reflux for 21/2 hours. The reaction mixture is then cooled, filtered, and concentrated to dryness by rotary evaporator, keeping exposure to moisture to a minimum. The crude product is re-dissolved in 100 mL THF, and the pH of the solution is adjusted to 5.5-6.0 by addition of pyridine. The product mixture is again filtered, and the product is purified by fractional distillation to give methyl 2-isocyanato-5-phenyl-4-pentenoate.
Workup
- customprepared
- temperatureThe reaction mixture is then heated
- temperatureat reflux for 21/2 hours
- temperatureThe reaction mixture is then cooled
- filtrationfiltered
- concentrationconcentrated to dryness by rotary evaporator
- dissolutionThe crude product is re-dissolved in 100 mL THF
- additionthe pH of the solution is adjusted to 5.5-6.0 by addition of pyridine
- filtrationThe product mixture is again filtered
- distillationthe product is purified by fractional distillation
Sources & evidence
- ORD record
- ord-8b862e1e08bc459d8f02bc2e20e36c6f
- Source dataset
- uspto-grants-1990_12
- Patent number
- US04977272
Reaction notes
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