HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239305Generated: October 31, 2026
Methanol → Methyl 4-(Benzyloxy)-2-methyl-1H-benzo[d]imidazole-6-carboxylate
https://huagongshe.com/reaction/2239305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(benzyloxy)-2-methyl-1H-benzo[d]imidazole-6-carboxylic acid | HCID 68574531 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(Benzyloxy)-2-methyl-1H-benzo[d]imidazole-6-carboxylate | HCID 68577093 | — |
Reaction Steps
A mixture of 2-methyl-4-[(phenylmethyl)oxy]-1H-benzimidazole-6-carboxylic acid (10.0 g, 35.4 mmol, STEP 4 in Example 1), and thionyl chloride (5.2 mL, 7.1 mmol) in methanol (300 mL) was stirred at 80° C. for 3 hours. The mixture was diluted with ethyl acetate, and washed with saturated ammonium chloride aqueous solution. The organic layer was dried over magnesium sulfate, and concentrated in vacuum. The residue was diluted with methanol, filtered to remove the precipitate, and the filtrate was concentrated in vacuum. The resulted solid was washed with dichloromethane to give the title compound as a brown solid (29.8 g, crude), which was used in the next step without further purification. MS (ESI) m/z: 297 (M+H)+, 295 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723321B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-7c690e24aec949af9893321babf744d2 |
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| Source note | uspto-grants-2010_05 |
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