Carbon Dioxide → Cyprodinil

HRID 358800Notes

Reaction equation

HRID 358800 reaction equation
C(=O)(O)O.[C:5]1([NH:11][C:12]([NH2:14])=[NH:13])[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[CH:15]1([C:18](=O)[CH2:19][C:20](=O)[CH3:21])[CH2:17][CH2:16]1.C(=O)=O>C(OCC)C>[C:5]1([NH:11][C:12]2[N:14]=[C:20]([CH3:21])[CH:19]=[C:18]([CH:15]3[CH2:17][CH2:16]3)[N:13]=2)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

Participants

5

Reactant 3

HCID 280Carbon DioxideHCID 110188691-Cyclopropyl-butane-1,3-dioneHCID 16217093Carbonic acid, compound with phenylguanidine (1:1)

Product 1

HCID 86367Cyprodinil

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

10 g (51 mmol) of phenylguanidine hydrogen carbonate and 9.7 g (77 mmol) of 1-cyclopropyl-1,3-butanedione are heated at 110° C. for 6 hours with stirring, the evolution of carbon dioxide which occurs subsiding as the reaction progresses. After the dark brown emulsion has been cooled to room temperature, 50 ml of diethyl ether are added and the mixture is washed twice with 20 ml of water each time, dried over sodium sulfate and filtered, and the solvent is evaporated. The dark brown oil which remains (=13.1 g) is purified by column chromatography over silica gel (diethyl ether/toluene: 5/3). After the eluant mixture has been evaporated off, the brown oil is made to crystallise and recrystallised from diethyl ether/petroleum ether at 30°-50° C. Light-brown crystals are obtained. Melting point: 67°-69° C.; yield: 8.55 g (38 mmol) (=74.5% of the theoretical yield).

Workup

  1. customas the reaction progresses
  2. washthe mixture is washed twice with 20 ml of water each time
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. customthe solvent is evaporated
  6. customis purified by column chromatography over silica gel (diethyl ether/toluene: 5/3)
  7. customAfter the eluant mixture has been evaporated off
  8. customto crystallise
  9. customrecrystallised from diethyl ether/petroleum ether at 30°-50° C
  10. customLight-brown crystals are obtained
  11. customyield: 8.55 g (38 mmol) (=74.5% of the theoretical yield)

Sources & evidence

ORD record
ord-a3dd463c1e5344bd87c9eb7a5e887993
Source dataset
uspto-grants-1991_03
Patent number
US04997941

Reaction notes

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