Synthesis 2024; 56(05): 771-776
DOI: 10.1055/a-2218-7443
paper

Mild Metal-Free 1,2-Dichlorination of Alkynes by NCS-PPh3-H2O System

Jianan Yuan
a   Division of Environmental Materials Science, Graduate School of Environmental Science, Hokkaido University, N10W5 Sapporo 060-0810, Japan
,
Nurcahyo Iman Prakoso
a   Division of Environmental Materials Science, Graduate School of Environmental Science, Hokkaido University, N10W5 Sapporo 060-0810, Japan
b   Chemistry Department, Universitas Islam Indonesia, Indonesia
,
Tatsuya Morozumi
a   Division of Environmental Materials Science, Graduate School of Environmental Science, Hokkaido University, N10W5 Sapporo 060-0810, Japan
c   Section of chemistry, Faculty of Science, Hokkaido University, N10W8 Sapporo 060-0810, Japan
,
Taiki Umezawa
a   Division of Environmental Materials Science, Graduate School of Environmental Science, Hokkaido University, N10W5 Sapporo 060-0810, Japan
d   Section of Environmental Material Science, Faculty of Environmental Earth Science, Hokkaido University, N10W5 Sapporo 060-0810, Japan
› Institutsangaben

This work was financially supported by Grant-in-Aid for Young Scientists (B) [23710245] and Grant-in-Aid for Scientific Research (C) [16K01908] from the Japan Society for the Promotion of Science (JSPS).


Abstract

Facile dichlorination of alkynes to give 1,2-dichloroalkenes is described. Previous studies for the synthesis of the 1,2-dichloroalkenes from the corresponding alkynes require stoichiometric amount of copper salt, preparation of the chlorinating reagent from hazardous compounds such as molecular chlorine, and highly acidic conditions. In this paper, only ubiquitous reagents, NCS-PPh3-H2O, are used to prepare the 1,2-dichloroalkenes from the alkynes under mild conditions. Various functional groups such as esters, ethers or carbamates were tolerated under these reaction conditions.

Supporting Information



Publikationsverlauf

Eingereicht: 15. September 2023

Angenommen nach Revision: 28. November 2023

Accepted Manuscript online:
28. November 2023

Artikel online veröffentlicht:
09. Januar 2024

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