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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764171Generated: November 2, 2026

Acetyl chloride → 3-[4-(4-Chlorophenoxy)phenyl]-3-hydroxybut-1-yne

https://huagongshe.com/reaction/1764171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chlorophenyl phenyl etherHCID 23436—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDimethyl SulfoxideHCID 679—
Product3-[4-(4-Chlorophenoxy)phenyl]-3-hydroxybut-1-yneHCID 20345599—

Reaction Steps

A solution of 2.47 g. of 4'-chloro-4-acetyldiphenyl ether, which can be prepared from 4-chlorodiphenyl ether and acetyl chloride in the presence of AlCl3, in 6 ml. of THF and 2 ml. of DMSO is added dropwise to a suspension of 1.38 g. of lithium acetylide/ethylenediamine complex in a mixture of 3 ml. of absolute THF and 4 ml. of absolute DMSO, while acetylene is bubbled through the mixture. The mixture is stirred for one hour while under nitrogen blanketing. An aqueous solution of ammonium chloride is added to the solution, which contains lithium 3-[4-(4-chlorophenoxy)phenyl]-but-1-yn-3-olate and the mixture is poured into water and worked up in the customary manner to give 3-[4-(4-chlorophenoxy)phenyl]-3-hydroxybut-1-yne, m.p. 55°-57°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115456
Source datasetuspto-grants-1978_09
ORD IDord-55bd1118a6504a99a0307940efb2f28d
Source noteuspto-grants-1978_09