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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232703Generated: November 1, 2026

Hydrochloric Acid → HCID 53834781, compound

https://huagongshe.com/reaction/2232703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant4-IodoanisoleHCID 69676—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 13849412HCID 13849412—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 53834781HCID 538347819%

Reaction Conditions

Temperature160 °C

Reaction Steps

A stirred mixture of 3,3-dimethyl-4-(4-fluoro-3phenoxybenzyloxy)but-1-ene (0.27 g), p-iodoanisole (0.21 g), palladium (II) diacetate (0.02 g), tri-o-toluylphosphine (0.054 g) and tetramethylethylenediamine (0.1 g) was heated at 160° C. for 24 hours. After cooling, the mixture was poured into dilute aqueous hydrochloric acid, and extracted into ethyl acetate, the extracts combined, washed with water, dried over anhydrous magnesium sulphate, and concentrated by evaporation of the solvent to yield a brown oil. The crude product was distilled through a kugelrohr apparatus to give 3,3-dimethyl-1-(4-methoxyphenyl)-4-(4-fluoro-3-phenoxybenzyloxy)but-1-ene (0.033 g), as an oil, containated by 30% of 3,3-dimethyl-2(4-methoxyphenyl)-4-(4-fluoro-3-phenoxybenzyloxy)but-1ene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788348
Source datasetuspto-grants-1988_11
ORD IDord-a6deebc6591e447e8d937fa97ce95631
Source noteuspto-grants-1988_11