Methanethiol → HCID 178484946, compound

HRID 917996Notes

Reaction equation

HRID 917996 reaction equation
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[IH:10].[CH3:11][NH:12][C:13](=[N:16][CH3:17])SC.CS>C(O)C>[IH:10].[CH3:11][NH:12][C:13]([NH:16][CH3:17])=[N:9][CH2:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Reactant 3

HCID 878MethanethiolHCID 1001PhenethylamineHCID 2775205Methyl N,N'-dimethylcarbamimidothioate--hydrogen iodide (1/1)

Product 1

HCID 178484946HCID 178484946, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

2-phenylethylamine (2.4 g.), N,N',S-trimethylisothiourea hydriodide (4.92 g.) and ethanol (70 ml.), were boiled together under reflux for eight hours; methyl mercaptan was evolved. The resulting solution was evaporated to dryness and the residue recrystallised from methanol/ether mixture to yield N,N'-dimethyl-N"-2-phenylethylguanidine hydriodide, melting point 156°-160°C.

Workup

  1. temperatureunder reflux for eight hours
  2. customThe resulting solution was evaporated to dryness
  3. customthe residue recrystallised from methanol/ether mixture

Sources & evidence

ORD record
ord-f4ee57d54bcb4c648d3450532234631c
Source dataset
uspto-grants-1976_07
Patent number
US03968243

Reaction notes

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