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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726506Generated: October 25, 2026

Tetrahydrofuran → HCID 178471409, compound

https://huagongshe.com/reaction/726506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant(3-(Ethoxycarbonyl)propyl)triphenylphosphonium BromideHCID 2773643—
ReactantNaHMDS tetrahydrofuranHCID 23700795—
ReactantHCID 178520918HCID 178520918—
SolventDiethyl EtherHCID 3283—
ProductHCID 178471409HCID 17847140962%

Reaction Steps

First, 25.7 g of 3-ethoxycarbonylpropyltriphenylphosphonium bromide, 10.1 g of trans-4-(2,3-difluorophenyl)cyclohexanecarbaldehyde, and 150 ml of dry tetrahydrofuran were placed in a 300 ml flask. Then, 56.3 ml of 1.0M sodium bis(trimethylsilyl)amide/tetrahydrofuran solution was added dropwise to the reaction mixture at -70° C. to -60° C. The reaction mixture was stirred while being allowed to warm to room temperature over 6 hours. Ether was added to the reaction mixture. The ether solution was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: toluene/hexane=1/1) to obtain 9.0 g of 2,3-difluoro-1-[trans-4-(4-ethoxycarbonyl-1-butenyl)cyclohexyl]benzene (Y: 62%). The compound thus obtained had a purity of 89.2% (mixture of E and Z isomers) by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05709911
Source datasetuspto-grants-1998_01
ORD IDord-5ce15233ac3344868d239d09bf7904c8
Source noteuspto-grants-1998_01