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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1396107Erstellt: 25. Oktober 2026

Acetic Anhydride → HCID 178471945, Verbindung

https://huagongshe.com/reaction/1396107

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktEthyl orthoformateHCID 31214—
EduktEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—
Edukt1-Amino-1-(2-hydroxypropan-1-yl)cyclobutaneHCID 55284401—
LösungsmittelTolueneHCID 1140—
ProduktHCID 178471945HCID 17847194583%

Reaktionsschritte

A stirred solution of ethyl 3-oxo-3-(2,3,4,5-tetrafluorophenyl)propionate (2.45 g, 9.27 mmol), Ac2O (5.30 mL, 56.1 mmol) and triethyl orthoformate (3.10 mL, 18.6 mmol) was heated at 120° C. for 3 hours. The mixture was concentrated in vacuo and dried under high vacuum. To 1-[1-aminocyclobutyl]-2-propanol (1.20 g, 9.29 mmol) in anhydrous toluene (10 mL) was slowly added to a mixture of the residue in anhydrous toluene (30 mL) at 0° C. and stirred at room temperature for 2 hours. The solvent was removed by evaporation. Flash chromatography (AcOEt:Hexane=1:1) of the residue gave the title compound as a pale yellow solid (3.10 g, 83%). 1H-NMR (400 MHz, CDCl3) δ 0.95 (0.6H, t, J=7.3 Hz), 1.09 (2.4H, t, J=7.3 Hz), 1.29 (3H, d, J=6.1 Hz), 1.51 (1H, brs), 1.83-2.05 (4H, m), 2.18-2.35 (3H, m), 2.41-2.53 (1H, m), 3.95-4.15 (3H, m), 6.96-7.13 (1H, m), 8.27 (0.8H, d, J=14.7 Hz), 8.31 (0.2H, d, J=14.7 Hz), 10.30 (0.2H, d, J=13.4 Hz), 11.56 (0.8H, d, J=13.4 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08901112B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-f49ea1a2fff14801bd0402a5ffed3eed
Quellennotizuspto-grants-2014_12