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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516652Generated: November 1, 2026

Water → HCID 66671882, compound

https://huagongshe.com/reaction/1516652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyltributylstannaneHCID 90628—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 86617901HCID 86617901—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 66671882HCID 66671882103.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

g of ethyl 3″-tert-butyl-4″-diethylamino-4′-trifluoromethanesulfonyloxy[1,1′;3′,1″]terphenyl-4-carboxylate (2 mmol) are dissolved at room temperature in 23 mL of dimethylformamide, and 250 mg of LiCl (6 mmol) and 0.74 mL of allyltributyltin (2.4 mmol) are then added. The reaction medium is heated and, at 40° C., 70 mg of dichlorobis(triphenylphosphine)palladium (0.1 mmol) are added and the reaction medium brought to 120° C. and stirred for 20 minutes. The reaction is stopped by adding 30 mL of water and then extracted with 30 mL of ethyl acetate. The organic phases are washed with 80 mL of water and then dried over magnesium sulfate. The solvents are evaporated off and the residue is then purified by chromatography on silica gel (eluent: heptane). 940 mg of ethyl 3″-tert-butyl-4″-diethylamino-4′-vinyl[1,1′;3′,1″]terphenyl-4-carboxylate are obtained (yield=100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227507B2
Source datasetuspto-grants-2012_07
ORD IDord-1bada1858c434d5681e2cc2dce9f5a73
Source noteuspto-grants-2012_07