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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463910Generated: October 30, 2026

HCID 86740358, compound → HCID 86740356, compound

https://huagongshe.com/reaction/463910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86740358HCID 86740358—
ReactantHCID 178418361HCID 178418361—
CatalystPd barium sulfateHCID 16218511—
SolventMethanolHCID 887—
ProductHCID 86740356HCID 8674035654.6%

Reaction Steps

In a manner analagous to Example 2, a solution of 3.42 g of (Z)-[5-(4-methoxy-2,3,6-trimethylphenyl)-3-methyl-2-penten-4-ynyl]triphenylphosphonium bromide in 240 ml of methanol was hydrogenated in the presence of 1.8 g of palladium/barium sulphate (5%). 188 ml of hydrogen were taken up within 2 hours. The crude product (3.4 g) of (2Z,4Z)-[5-(4-methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadienyl]triphenylphosphonium bromide (chemical yield 54.6% in accordance with HPLC) obtained after filtration and evaporation was dissolved in 20 ml of methylene chloride and crystallized by the dropwise addition of 50 ml of ethyl acetate while stirring. The suspension was left to stand at 0° C. overnight and filtered. The crystals were washed with a small amount of ethyl acetate/methylene chloride (volume ratio 5:1) and dried at room temperature/0.01 mbar. There was thus obtained 1.0 g of 94.9% (2Z,4Z)-[5-(4-methoxy-2,3,6-trimethylphenyl)-3-methyl-2,4-pentadienyl]triphenylphosphonium bromide; m.p. 202°-205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544770
Source datasetuspto-grants-1985_10
ORD IDord-bd9f1f3c26a14881b1adf6bb0b693689
Source noteuspto-grants-1985_10