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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342359Generated: November 1, 2026

Water → HCID 178439112, compound

https://huagongshe.com/reaction/342359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantT0400-2412HCID 11102709—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178439113HCID 178439113—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178439112HCID 17843911260.4%

Reaction Steps

Suspension of 11.8 g of 4-chlorobenzyltriphenyl-phosphonium bromide in 100 ml of THF was stirred under nitrogen gas stream, and 2.8 g of potassium-t-butoxide was added to the suspension at room temperature. After stirred at room temperature for 1 hour, a solution of 7 g of the 4-(2-(trans-4-(4-n-propylphenyl)cyclohexyl)ethyl)benzaldehyde in 50 ml of THF was added dropwise. After stirred at room temperature for 2 hours, 300 ml of water was added and extracted with 300 ml of ethyl acetate. Organic layer was washed with water and dried over anhydrous magnesium sulfate, the solvent was distilled off under a reduced pressure, and then 200 ml of heptane was added. Precipitate thus separated was filtered off, and subjected to a column chromatography over a silica gel by using ethyl acetate/heptane (1/5) as an eluent. Solvent was distilled off under a reduced pressure to obtain 5.6 g 4-(2-(4-(2-(trans-4-(4-n-propylphenyl)cyclohexyl)ethyl)phenyl)ethenyl)chlorobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05858275
Source datasetuspto-grants-1999_01
ORD IDord-4e361b0acd8146c5bdcbf87512adb869
Source noteuspto-grants-1999_01