HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16700Generated: October 25, 2026
Hydrochloric Acid → HCID 178501253, compound
https://huagongshe.com/reaction/16700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Reactant | HCID 178501210 | HCID 178501210 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178501253 | HCID 178501253 | — |
Reaction Steps
Methyl trans-4-aminocyclohexanecarboxylate hydrochloride (4.08 g) obtained in Reference Example 2(1) is suspended in chloroform (50 ml), and thereto is added triethylamine (8.8 ml) under ice-cooling. Subsequently, a solution of 3-chloropropanesulfonyl chloride (3.35 ml) in chloroform (20 ml) is added dropwise over 20 minutes under the same temperature. After stirring for 2 hours at room temperature, 5% hydrochloric acid is added to the reaction solution and the mixture is extracted with chloroform. The organic layer is washed with saturated brine, dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. The resulting residue is suspended in diisopropylamine, and filtered to collect precipitates to give methyl trans-4-{[(3-chloropropyl)sulfonyl]amino}cyclohexanecarboxylate (6.14 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737161B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-f13ca10a3f374ab6b0ddea3ebea60e36 |
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| Source note | uspto-grants-2010_06 |
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