HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388649Generated: October 26, 2026
Water → 3-(1-(4-Chloro-2,5-dimethylphenylsulfonyl)piperidin-2-yl)propionic Acid Ethyl Ester
https://huagongshe.com/reaction/2388649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-2,5-dimethylbenzenesulfonyl chloride | HCID 18617291 | — |
| Reactant | 7599-21-5 | HCID 19261412 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(1-(4-Chloro-2,5-dimethylphenylsulfonyl)piperidin-2-yl)propionic Acid Ethyl Ester | HCID 57916246 | — |
Reaction Steps
Triethylamine (30 g) was added dropwise to a solution of 3-(piperidin-2-yl)propionic acid ethyl ester hydrochloride (30 g) in methylene chloride (210 ml) at 0° C. and the mixture was then stirred at room temperature for 10 minutes. Chloro-2,5-dimethylbenzene-1-sulfonyl chloride (32.3 g) was then added slowly and the mixture was stirred for 2 hours. The reaction was observed by thin layer chromatography. Because of incomplete conversion, the mixture was stirred for a further 17 hours before the reaction was ended by addition of water (200 ml). The phases were separated and the aqueous phase was extracted with MC (150 ml). The combined organic phases were dried with Na2SO4, filtered and concentrated in vacuo. Purification of the crude product was carried out by chromatography on silica gel (5% ethyl acetate in hexane). The yield was 47.23 g (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268814B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-1440a6162b8249cabd96e8d641874358 |
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| Source note | uspto-grants-2012_09 |
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