HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197440Generated: October 31, 2026
Chloroacetyl chloride → HCID 52952411, compound
https://huagongshe.com/reaction/2197440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86654171 | HCID 86654171 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 52952411 | HCID 52952411 | 95% |
Reaction Steps
168 mg (1 eq.) of 4-(3-thiophen-2-yl[1,2,4]oxadiazol-5-yl)-piperidinium hydrochloride obtained in step 1) above and 220 μl (3.1 eq.) of triethylamine were dissolved in 1 ml of dichloromethane and stirred at a temperature of −15° C. A solution of chloroacetyl chloride (40 μl, 1 eq.) in 1 ml of dichloromethane (CH2Cl2) was added dropwise to the resulting suspension. The resulting mixture was stirred at room temperature for 2 hours. 20 ml of dichloromethane were then added, and the resulting organic phase was washed with three times 50 ml of 5% hydrochloric acid and then dried over MgSO4, filtered and evaporated. 2-Chloro-1-[4-(3-thiophen-2-yl[1,2,4]oxa-diazol-5-yl)piperid-1-yl]ethanone was obtained in the form of a white solid, in a yield of 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338599B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-a1a484ab68cf4ab5858b809a13d501fb |
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| Source note | uspto-grants-2012_12 |
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