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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080569Generated: November 3, 2026

Tetrahydrofuran → HCID 23364881, compound

https://huagongshe.com/reaction/1080569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 22369354HCID 22369354—
ReactantHCID 178505964HCID 178505964—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 23364881HCID 2336488185.1%

Reaction Steps

40 ml of a tetrahydrofuran solution of 0.8 moles of 3,4,5-trifluorophenylzinc chloride prepared by reaction between a corresponding Grignard reagent and zinc chloride was dropped in a mixture of 10.0 g of (2-fluoro-4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)phenyl) trifluoromethanesulfonate, 100 mg of tetrakis(triphenylphosphine)palladium (0), 500 mg of lithium chloride and 50 ml of N,N-dimethylformamide. After agitation at 50° C. for 8 hours, the mixture was charged into an ammonium chloride aqueous solution, followed by extraction with ethyl acetate. The ethyl acetate solution was washed with brine, dried, and concentrated, followed by purification of the resultant residue through silica gel chromatography to obtain 8.20 g (yield: 75%) of 4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)-2,3',4',5'-tetrafluorobiphenyl. The results of IR and 1H-NMR analyses of the product are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05582765
Source datasetuspto-grants-1996_12
ORD IDord-90bb6ece3d68451eb28f14cdfc083a9b
Source noteuspto-grants-1996_12