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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26550Generated: October 26, 2026

Hydrochloric Acid → Ethyl 3-fluoro-4-cyclohexylphenylglyoxylate

https://huagongshe.com/reaction/26550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoric AcidHCID 7628—
ReactantHydrofluoric AcidHCID 14917—
ReactantEthyl 3-amino-4-cyclohexylphenylglyoxylateHCID 20515218—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductEthyl 3-fluoro-4-cyclohexylphenylglyoxylateHCID 20515163—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150148
Source datasetuspto-grants-1979_04
ORD IDord-13819aa5c15a4278b384dc412c9210ad
Source noteuspto-grants-1979_04