Martin A Berliner, Katherine Belecki
Index: J. Org. Chem. 70(23) , 9618-21, (2005)
Full Text: HTML
[Reaction: see text]. Zinc(II) salts catalyze the reaction between acetals and acid halides to provide haloalkyl ethers in near-quantitative yield. Reactions from millimole to mole scale are typically complete in 1-4 h with 0.01 mol % catalyst. The solutions of haloalkyl ethers thus obtained can be utilized directly in reactions in which the presence of the ester byproduct does not interfere. Excess haloalkyl ether is destroyed on workup, thereby minimizing exposure to this class of carcinogenic compounds.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
![]() |
Chloromethyl methyl ether
CAS:107-30-2 |
C2H5ClO |
|
Solid-phase microextraction fiber development for sampling a...
2014-01-01 [J. Environ. Health. Sci. Eng. 12(1) , 123, (2014)] |
|
[Organometallics 25 , 4909, (2006)] |
|
Bis(chloromethyl) ether and technical-grade chloromethyl met...
2011-01-01 [Rep. Carcinog. 12 , 71-3, (2011)] |
|
Bis(Chloromethyl) ether and technical-grade chloromethyl met...
2004-01-01 [Rep. Carcinog. 11 , III56-7, (2004)] |
|
Reactive chemicals and cancer.
1997-05-01 [Cancer Causes Control 8(3) , 473-90, (1997)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2026 ChemSrc All Rights Reserved
