HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840775Generated: October 31, 2026
Thionyl Chloride → HCID 70170438, compound
https://huagongshe.com/reaction/840775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22620335 | HCID 22620335 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 70170438 | HCID 70170438 | — |
Reaction Steps
Thionyl chloride (2 ml) is added to a chloroform solution (30 ml) of 1-(biphenyl-4-ylmethyl)-6-hydroxymethyl-2-methylbenzimidazole (3.62 g), and the solution is stirred for one hour at 60° C. A sodium bicarbonate aqueous solution is added and the reaction is halted. The chloroform layer is washed with water and dried. After removing the solvent through evaporation under reduced pressure, ethyl acetate is added and crystallization is performed. After the crystals are separated through filtration and washed with ethyl acetate, they are dried and thus, 1-(biphenyl-4-ylmethyl)-6-chloro-methyl-2-methylbenzimidazole (2.04 g) is obtained. 1H-NMR (CDCl3, δ): 2.67 (3H, s), 4.71 (2H, s), 5.40 (2H. s), 7.12 (2H, d, J=8.2 Hz), 7.31-7.38 (3H, m), 7.43 (3, s), 7.52-7.58 (4H, m), 7.75 (1H, d, J=8.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369092B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-faa512c2a7e04378b328e76e2f98c42d |
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| Source note | uspto-grants-2002_04 |
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