1961
DOI: 10.1021/ie50614a011
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SAFETY—Stabilizing Isopropyl Ether Against Peroxidation

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Cited by 3 publications
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“…In the historical process, isolation of chloroallyl ester 8a , was accomplished by trituration with isopropyl ether (Scheme ). This is not ideal, due to the tendency of this solvent to form hazardous peroxides during storage . As a result, our second-generation process involved a direct drop isolation of 8b using MtBE as a cosolvent (with THF and AcOH).…”
Section: Resultsmentioning
confidence: 99%
“…In the historical process, isolation of chloroallyl ester 8a , was accomplished by trituration with isopropyl ether (Scheme ). This is not ideal, due to the tendency of this solvent to form hazardous peroxides during storage . As a result, our second-generation process involved a direct drop isolation of 8b using MtBE as a cosolvent (with THF and AcOH).…”
Section: Resultsmentioning
confidence: 99%
“…In the case ofW thiocyanate also, it can be extracted with amyl acetate, n-amyl alcohol, butyl acetate cyclohexanol, ethyl acetate, ethyl ether, isopropylether and tributylphosphate, lsopropylether has got an edge over others, as it gives better phase separation. Dasler and Bauer (1946) and Hamstead et al (1961) recommended the purification of the organic solvents used for the extraction of tungsten-thiocyanate complex to eliminate organic peroxides, which prevent distinct separation of the phases. Extraction of W(VI) from 1 M HC1 with 12 M lithium chloride (as salting agent) into mesityl oxide has been carried out by Shinde and Khopkar (1969).…”
Section: Separation Followed By Spectrophotometrymentioning
confidence: 99%