HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579759Generated: October 30, 2026
Methyl chloroformate → HCID 70414805, compound
https://huagongshe.com/reaction/579759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 1,2,3,9-Tetrahydro-3-[(2-methyl-1H-imidazol-1-yl)methyl]-4H-carbazol-4-one | HCID 10891224 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70414805 | HCID 70414805 | — |
Reaction Steps
Sodium hydride (0.075 g) was added to a solution of 1,2,3,9-tetrahydro-3-[(2-methyl-1H-imidazol-1-yl)methyl]-4H-carbazol-4-one (0.7 g) in dimethylformamide (10 ml) and the mixture was stirred at room temperature for 30 min. Methyl chloroformate (0.3 ml) was added and stirring continued at room temperature for 4 h. The resulting solution was basified with sodium carbonate (100 ml) filtered, and the filtrate was extracted with ethyl acetate (2×50 ml). The combined organic extracts and solid were washed with water (3×50 ml), dried (Na2SO4) and evaporated in vacuo to give a solid. Purification by flash chromatography (A) gave a solid, which was dissolved in ethanol (5 ml) and added to a solution of maleic acid (0.018 g) in ethanol (5 ml) to give the title compound (0.07 g) m.p. 91°-92°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749718 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-6a7c0845b6894197b0a641754889d432 |
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| Source note | uspto-grants-1988_06 |
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