HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1704464Erstellt: 24. Oktober 2026
Triethylamine → 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate
https://huagongshe.com/de/reaction/1704464
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one | HCID 3017358 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate | HCID 86735359 | 53% |
Reaktionsschritte
To a stirred and cooled (ice-water bath) mixture of 14.1 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one, 8 parts of N,N-diethylethanamine and 195 parts of dichloromethane are added dropwise 7.8 parts of methanesulfonyl chloride. Upon completion, stirring is continued first for 15 minutes while still cooling an further for 1 hour at reflux temperature. The dichloromethane is evaporated and the residue is dissolved in 4-methyl-2-pentanone and water while heating. The layers are separated and the organic phase is stirred with 100 parts of water, while cooling in an ice-bath. The precipitated product is filtered off and dried, yielding 10 parts (53%) of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate; mp. 140° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04126687 |
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| Quelldatensatz | uspto-grants-1978_11 |
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| ORD ID | ord-502e2b96607a4e4fa642f3e11b310819 |
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| Quellennotiz | uspto-grants-1978_11 |
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