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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249048Erstellt: 25. Oktober 2026

Triethylamine → Methyl 1-((acetylthio)methyl)cyclopropaneacetate

https://huagongshe.com/reaction/249048

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktMethanesulfonateHCID 85257—
EduktSodium BicarbonateHCID 516892—
Edukt(1-Hydroxymethylcyclopropyl)acetic acid methyl esterHCID 29941748—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 1-((acetylthio)methyl)cyclopropaneacetateHCID 53482060—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

To a solution of the alcohol of Step 10 (28.2 g, 0.20 mol) and triethylamine (82 mL, 0.59 mol) in dichloromethane (1L) 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212180
Quelldatensatzuspto-grants-1993_05
ORD IDord-f0cec03e94b74c9d8e2de5b44b762c09
Quellennotizuspto-grants-1993_05