Methyl iodide → HCID 20506295, compound

HRID 2050261Notes

Reaction equation

HRID 2050261 reaction equation
[SH:1][C:2]1[N:6]([CH2:7][CH2:8][CH2:9][OH:10])[C:5]2[CH:11]=[CH:12][CH:13]=[CH:14][C:4]=2[N:3]=1.I[CH3:16]>CO>[CH3:16][S:1][C:2]1[N:6]([CH2:7][CH2:8][CH2:9][OH:10])[C:5]2[CH:11]=[CH:12][CH:13]=[CH:14][C:4]=2[N:3]=1

Participants

4

Procedure

A mixture of 20.8 parts of 2-mercapto-1H-benzimidazole-1-propanol, 15.62 parts of iodomethane and 120 parts of methanol is stirred overnight at room temperature. The reaction mixture is evaporated and the residue is dissolved in 500 parts of water. The solution is filtered over hyflo and the filtrate is alkalized with solid potassium hydroxide. The oily product is extracted with trichloromethane. The extract is dried, filtered and evaporated, yielding 2-(methylthio)-1H-benzimidazole-1-propanol as a residue.

Workup

  1. customThe reaction mixture is evaporated
  2. dissolutionthe residue is dissolved in 500 parts of water
  3. filtrationThe solution is filtered over hyflo
  4. extractionThe oily product is extracted with trichloromethane
  5. customThe extract is dried
  6. filtrationfiltered
  7. customevaporated

Sources & evidence

ORD record
ord-2da80f680c6f412ba524eef632816a07
Source dataset
uspto-grants-1980_04
Patent number
US04200641

Reaction notes

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