HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 326942Erstellt: 25. Oktober 2026
Triethylamine → Methyl 1-((acetylthio)methyl)cyclopropaneacetate
https://huagongshe.com/reaction/326942
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | Methanesulfonate | HCID 85257 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | (1-Hydroxymethylcyclopropyl)acetic acid methyl ester | HCID 29941748 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 1-((acetylthio)methyl)cyclopropaneacetate | HCID 53482060 | — |
Reaktionsschritte
To a solution of the alcohol of Step 4 (28.2 g, 0.20 mol) and triethylamine (82 mL, 0.59 mol) in dichloromethane (1 L) cooled to -40° C. was added methanesulfonyl chloride (43.5 mL, 0.3 mol). The reaction mixture was warmed to -10° C. for 20 min and then an aqueous solution of NaHCO3 was added. The product was extracted with CH2Cl2, washed with brine and dried over Na2SO4. A portion of this mesylate (0.053 mol) was then dissolved in DMF (180 mL) and cooled to 0° C. Freshly prepared cesium thiol acetate (J. Org. Chem., 51, 3664, (1986)) (22 g, 0.11 mol) was added and the mixture was stirred overnight at r.t. The reaction mixture was poured into an aqueous solution of NaHCO3 and extracted with Et2O. The organic phases were washed with brine and dried over Na2SO4. The residual oil was then purified by flash chromatography with 10:1 hexane:EtOAc to yield 7.5 g, 70%, of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05270324 |
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| Quelldatensatz | uspto-grants-1993_12 |
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| ORD ID | ord-c7a5d75aec7f44b6a51c59dab759c847 |
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| Quellennotiz | uspto-grants-1993_12 |
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