Ethanol → HCID 178520824, compound

HRID 2050260Notes

Reaction equation

HRID 2050260 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][CH2:9][CH2:10][CH2:11][OH:12].[OH-].[K+].C(O)C.[C:18](=S)=[S:19]>O>[SH:19][C:18]1[N:8]([CH2:9][CH2:10][CH2:11][OH:12])[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[N:1]=1

Participants

6

Procedure

To a stirred mixture of 93 parts of 3-(2-aminophenyl)amino-1-propanol, 45.5 parts of potassium hydroxide and 600 parts of an ethanol solution 85% in water are added dropwise 60.8 parts of carbon disulfide. Upon completion, stirring is continued for 6 hours at reflux temperature. The reaction mixture is evaporated and the residue is taken up in 1500 parts of water. The whole is filtered over hyflo and the filtrate is acidified with acetic acid. The oily product solidifies on scratching. It is filtered off, washed with water and dried, yielding 2-mercapto-1H-benzimidazole-1-propanol; mp. 110° C.

Workup

  1. temperatureat reflux temperature
  2. customThe reaction mixture is evaporated
  3. filtrationThe whole is filtered over hyflo
  4. filtrationIt is filtered off
  5. washwashed with water
  6. customdried

Sources & evidence

ORD record
ord-afc650b425ab48e2993603bd6f558750
Source dataset
uspto-grants-1980_04
Patent number
US04200641

Reaction notes

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