HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649181Generated: October 30, 2026
Sodium Hydroxide → 4-Allyloxy-8(2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinoline
https://huagongshe.com/reaction/649181
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-Allyloxy-8-bromo-3-methyl-5,6,7,8-tetrahydroquinoline | HCID 14155523 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Allyloxy-8(2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinoline | HCID 14155524 | — |
Reaction Steps
0.46 Gram of 2-chlorobenzimidazole, 0.2 g of thiourea and 10 ml of ethanol were mixed together and the mixture was refluxed for 2 hours. To this reaction mixture was added 0.62 g of 4-allyloxy-8-bromo-3-methyl-5,6,7,8-tetrahydroquinoline and 0.3 g of sodium hydroxide, then the whole reaction mixture was refluxed for 5 hours. After the reaction was completed, ethanol was removed by evaporation, and to the residue thus obtained was added water and then extracted with chloroform, and the chloroform extract was dried with anhydrous magnesium sulfate, and the chloroform was removed by evaporation. The residue thus obtained was purified by means of a silica gel column chromatography (eluent: methylene chloride/methanol=100/1) to obtain 0.5 g of 4-allyloxy-8-(2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinoline in the form of light brown oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04738970 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-738f98f2012b485b8a5241fbc8b2bf8c |
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| Source note | uspto-grants-1988_04 |
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