HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593006Generated: November 1, 2026
Acetyl chloride → 4-(3-Methyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride
https://huagongshe.com/reaction/1593006
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,1-Dimethylethyl 4-(3-methyl-1,2,4-oxadiazol-5-yl)-1-piperidinecarboxylate | HCID 21098360 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(3-Methyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride | HCID 45791888 | 55% |
Reaction Steps
Crude tert-butyl 4-(3-methyl-1,2,4-oxadiazol-5-yl)piperidine-1-carboxylate (5.73 g, 21.3 mmol) was dissolved in MeOH (100 mL) and a premixed solution of acetyl chloride (1.53 mL, 42.8 mmol) in MeOH (10 mL) was added and the mixture heated to 60° C. for 1 hour, then the solvents were evaporated and the resultant gum triturated with dichloromethane/diethyl ether (1:1) to give a cream solid which was filtered, washed with diethyl ether and dried, to give the title compound as a solid (1.98 g, 55% yield); MS: 168 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294636B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-b51cf27fcf4f48e2be4bf1cc431a7188 |
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| Source note | uspto-grants-2007_11 |
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