HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649473Generated: November 2, 2026
1,4-Dichlorobutane → 8-(2-Pyrimidinyl)-8-aza-5-azoniaspiro[4.5]decane chloride
https://huagongshe.com/reaction/1649473
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dichlorobutane | HCID 8059 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(2-Pyrimidinyl)piperazine | HCID 88747 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-(2-Pyrimidinyl)-8-aza-5-azoniaspiro[4.5]decane chloride | HCID 13054188 | 70% |
Reaction Steps
A mixture of 1-(2-pyrimidinyl)piperazine (32.8 g., 0.2 mole), 1,4-dichlorobutane (76.2 g., 0.6 mole) and finely powdered sodium carbonate (44.5 g., 0.42 mole) in 300 ml. of acetonitrile is stirred and refluxed for a 12-hour period. The hot reaction mixture is filtered and the filter cake washed with 50-100 ml.of hot acetonitrile. Combined filtrates are maintained at room temperature until crystallization occurs, then cooled, filtered, and collected material washed with acetone to provide a 70-90% yield of 8-(2-pyrimidinyl)-8-aza-5-azoniaspiro[4.5]decane chloride. This material is hygroscopic and after drying under vacuum at room temperature affords the monohydrate form melting about 90° C. which on continued drying under vacuum at 90° C. for several hours affords the anhydrous product having a melting point of about 210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04417049 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-7b03672d50d24bb1902404fd71ada883 |
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| Source note | uspto-grants-1983_11 |
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