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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1063622Erstellt: 27. Oktober 2026

Trifluoromethanesulfonic anhydride → HCID 178500919, Verbindung

https://huagongshe.com/reaction/1063622

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoromethanesulfonic anhydrideHCID 67749—
Edukt2,6-Di-tert-butylpyridineHCID 68510—
EduktPropanoic acid, 3-hydroxy-, methyl esterHCID 80252—
EduktHCID 178484845HCID 178484845—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelNitromethaneHCID 6375—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelPotassium bisulfateHCID 516920—
ProduktHCID 178500919HCID 17850091995,7%

Reaktionsschritte

At 0° C. to a solution of 0.62 g (5.9 mmol) of methyl beta-hydroxypropionate in 4.5 mL of CH2Cl2 was added 1.4 mL (6.4 mmol, 2.4 eq) of 2,6-di-tert-butylpyridine, followed by 1.03 mL (6.2 mmol, 2.4 eq) of trifluoromethane sulfonic acid anhydride. The solution was stirred at that temperature for 2.5 h, was concentrated, and the residue was dissolved in 5 mL of nitromethane. To this solution 1 g (2.96 mmol) of trans-N-(4-hydroxy-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide and 1.3 mL (5.9 mmol, 2.0 eq) of 2,6-di-tert-butylpyridine in 10 mL of nitromethane were added. The solution was stirred at 60° C. for 3 h, diluted with EtOAc and 1M KHSO4. The inorganic phase was extracted with EtOAc, the combined organic phases were washed with a saturated aqueous solution of NaHCO3, brine and were dried over Na2SO4 and evaporated. Column chromatography on silica gel with EtOAc/n-hexane 1:3 gave 1.2 g (95%) of trans-3-{4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-propionic acid methyl ester as light yellow oil, MS: 424 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06965048B2
Quelldatensatzuspto-grants-2005_11
ORD IDord-0ab0dbe7d73b40679dc1f0b713d0a990
Quellennotizuspto-grants-2005_11