HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109055Generated: October 26, 2026
Chloroacetyl chloride → HCID 178501221, compound
https://huagongshe.com/reaction/2109055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178501220 | HCID 178501220 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178501221 | HCID 178501221 | — |
Reaction Steps
Methyl trans-4-({2-[(t-butoxycarbonyl)amino]ethyl}amino)cyclohexanecarboxylate (785 mg) obtained in Reference Example 71 (1) is dissolved in chloroform (8 ml), and thereto are added triethylamine (1.82 ml) and chloroacetyl chloride (249 μl) under ice-cooling. The mixture is then stirred at room temperature for 2 hours. The reaction solution is cooled with ice again, and chloroacetyl chloride (62 μl) is supplied thereto. The mixture is stirred at room temperature for 1 hour. To the reaction solution, saturated aqueous sodium hydrogen carbonate solution is poured and the mixture is extracted with chloroform. The organic layer is washed with water and saturated brine successively, dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. The resulting residue is purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1, followed by 1/1) to give methyl trans-4-[{2-[(t-butoxycarbonyl)amino]ethyl}-(chloroacetyl)amino]cyclohexanecarboxylate (568 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514449B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-45417a77ae9b495393b27332895646cf |
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| Source note | uspto-grants-2009_04 |
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