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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789457Generated: October 26, 2026

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

https://huagongshe.com/reaction/1789457

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 via 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 numberUS04689341
Source datasetuspto-grants-1987_08
ORD IDord-93abc6b367ac4c85828867dcc8b49366
Source noteuspto-grants-1987_08