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Methyl Isocyanate → HCID 152749587, compound

HRID 1284136
Notes
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Reaction equation

HRID 1284136 reaction equation
[CH3:1][N:2]=[C:3]=[O:4].[CH2:5]([O:7][C:8]([NH:10][C:11]([NH2:13])=[NH:12])=[O:9])[CH3:6]>O1CCOCC1>[CH3:1][NH:2][C:3]([NH:13][C:11]([NH:10][C:8]([O:7][CH2:5][CH3:6])=[O:9])=[NH:12])=[O:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 12228Methyl IsocyanateHCID 178473545HCID 178473545, compound

Product 1

HCID 152749587HCID 152749587, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

5.1 parts by weight of methylisocyanate were added to a suspension of 10 parts by weight of ethoxycarbonylguanidine (manufactured according to Isr. J. Chem. 8, 651 [1970] ) in 60 parts by volume of anhydrous dioxane, in the course of which the temperature rose to 45°C and the precipitate dissolved. After a short time, a crystalline precipitate separated out again, which was filtered off after cooling and washed with ether. It was dried in vacuo over P2O5 and paraffin chips.

Workup

  1. customrose to 45°C
  2. dissolutionthe precipitate dissolved
  3. customAfter a short time, a crystalline precipitate separated out again
  4. filtrationwhich was filtered off
  5. temperatureafter cooling
  6. washwashed with ether
  7. dry with materialIt was dried in vacuo over P2O5 and paraffin chips

Sources & evidence

ORD record
ord-57820e630b364996b0cf8005bfb08923
Source dataset
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03978056

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes