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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975616Generated: November 1, 2026

Tetrahydrofuran → HCID 178471528, compound

https://huagongshe.com/reaction/1975616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium HydroxideHCID 14797—
Reactant4-(4-Bromophenyl)cyclohexane-1-carbaldehydeHCID 19097901—
SolventWaterHCID 962—
ProductHCID 178471528HCID 178471528—

Reaction Steps

A mixture of 9.1 g of 4-(4-bromophenyl)cyclohexanecarb-oxaldehyde and 3.8 g of powdered potassium hydroxide in 200 ml of tetrahydrofuran was placed at room temperature in a sulphonation flask while gassing with argon and treated with 9.2 g of triethyl phosphonoacetate within 15 minutes, stirred overnight, taken up in 100 ml of water and extracted three times with 100 ml of methylene chloride each time. The organic phases were washed twice with 100 ml of water each time, dried over magnesium sulphate and concentrated. Low-pressure chromato-graphy of the residue (12 g) on silica gel with hexane/ethyl acetate (vol. 9:1) gave 11.7 g of ethyl (E)-3-[trans-4-(4-bromo-phenyl)cyclohexyl]acrylate as colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288428
Source datasetuspto-grants-1994_02
ORD IDord-088a694ada344cf3aeb140b8ff18f938
Source noteuspto-grants-1994_02