Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 839401Erstellt: 23. Oktober 2026

Hydrochloric Acid → Ethyl 3-fluoro-4-cyclohexylphenylglyoxylate

https://huagongshe.com/de/reaction/839401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBoric AcidHCID 7628—
EduktHydrofluoric AcidHCID 14917—
EduktEthyl 3-amino-4-cyclohexylphenylglyoxylateHCID 20515218—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
ProduktEthyl 3-fluoro-4-cyclohexylphenylglyoxylateHCID 20515163—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To 44.2 g. (0.15 moles) of ethyl 3-amino-4-cyclohexylphenylglyoxylate is added at 0° C 44 ml. of 1.5 moles of concentrated hydrochloric acid. The reaction mixture is maintained at 0° C and the diazonium salt is prepared with 23.2 g. (0.32 moles) of 95% sodium nitrite in 80 ml. of water. To this mixture is rapidly added a solution of 10.4 g. (0.17 moles) of boric acid dissolved in 22 g. (0.66 moles) of 60% hydrofluoric acid. The reaction mixture is then stirred for 1/2 hour and filtered, washed with 3 × 25 ml. of water, 2 × 25 ml. of methanol and 25 ml. of ether. The residual cake is then treated in vacuo. The treated cake is then placed in a distilling flask and heated to permit spontaneous decomposition. After the decomposition, the residue is then fractionally distilled to obtain ethyl 3-fluoro-4-cyclohexylphenylglyoxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04094995
Quelldatensatzuspto-grants-1978_06
ORD IDord-7f401b64c86b498a938349ce52a35892
Quellennotizuspto-grants-1978_06