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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65235Generated: October 25, 2026

1-(4-Chlorophenyl)-2-butyn-1-ol → (Z)-1-(4-chlorophenyl)-2-buten-1-ol

https://huagongshe.com/reaction/65235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Chlorophenyl)-2-butyn-1-olHCID 20188339—
CatalystLindlars catalystHCID 131709914—
Product(Z)-1-(4-chlorophenyl)-2-buten-1-olHCID 67901371—

Reaction Steps

Under nitrogen, hydrogenate a mixture of 10 g (0.055 mole) of 1-(4-chlorophenyl)-2-butyn-1-ol and 0.6 g Lindlar catalyst. Following the reaction vic NMR the reaction is complete in about two days. The hydrogenation is stopped and the reaction stirred under N2 at room temperature overnight. Filter off the catalysts, wash with methylene chloride combine the filtrate and evaporate to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613609
Source datasetuspto-grants-1986_09
ORD IDord-1ba35f007e7240af90d3407e16dabfe8
Source noteuspto-grants-1986_09