Hydrochloric Acid → HCID 178488138, compound
Reaction equation
[SH:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:4]=2[N:3]=1.[OH-].[K+].I[CH3:16].Cl>O.C(O)C>[CH3:16][S:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:4]=2[N:3]=1Participants
Conditions
- Temperature
- 5 °C
Procedure
First, 18.00 g (100 mmol) of 2-mercapto-5-methoxy-1H-benzimidazole, 16.83 g (300 mmol) of potassium hydroxide, 75 ml of ethanol, and 50 ml of water were added to a 3-necked flask (300 ml volume) equipped with a thermometer, a mechanical stirrer and a dropping funnel, and cooled to 5° C. Next, 15.00 g (105 mmol) of iodomethane was added dropwise to this solution over a period of 30 minutes while keeping internal temperature at 10° C. or lower. Then the solution was agitated for 2 hours at 10° C. or lower. The reaction solution was neutralized with an aqueous 2N hydrochloric acid solution, then the ethanol was removed under reduced pressure to precipitate a colorless solid. This solid was filtered and dried under reduced pressure to give 19.19 g of 2-methylthio-5-methoxy-1H-benzimidazole (yield of 98.9%).
Workup
- customequipped with a thermometer, a mechanical stirrer and a dropping funnel
- customat 10° C.
- customthe ethanol was removed under reduced pressure
- customto precipitate a colorless solid
- filtrationThis solid was filtered
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-7fe2fab725334d54803f2deb8b2530b7
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06197962B1
Reaction notes
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