HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168909Generated: October 30, 2026
Methyl chloroformate → HCID 58355341, compound
https://huagongshe.com/reaction/2168909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58355120 | HCID 58355120 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58355341 | HCID 58355341 | — |
Reaction Steps
1-(4-Methoxybutyl)-4,5,6,7-tetrahydro-1H-benzimidazole (625 mg) was dissolved in acetonitrile (5 ml), and the mixture was cooled to −15° C. Triethylamine (1.25 ml) and methyl chlorocarbonate (691 μl) were added dropwise. The reaction mixture was heated to room temperature and stirred for 12 hr. The reaction mixture was again cooled to −15° C., triethylamine (1.25 ml) and methyl chlorocarbonate (691 μl) were added dropwise, heated to room temperature and stirred for 12 hr. This operation was further repeated 3 times, aqueous sodium bicarbonate was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to basic silica gel column chromatography, and a fraction eluted with ethyl acetate was concentrated under reduced pressure to give the object product (225 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045436B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-39b4c2548ff04d50b9b205dbae66cbea |
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| Source note | uspto-grants-2015_06 |
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