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filingDate 1995-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_101bee3b4ff24adeea5af03ea17805b6
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publicationDate 1997-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5679576-A
titleOfInvention Gas chromatographic analysis of fluoromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether
abstract PCT No. PCT/JP95/00538 Sec. 371 Date Dec. 5, 1995 Sec. 102(e) Date Dec. 5, 1995 PCT Filed Mar. 23, 1995 PCT Pub. No. WO95/27898 PCT Pub. Date Oct. 19, 1995The present invention provides a method in which organic matter in the product accompanied with a non-reacted hydrogen fluoride can be handled without damaging the apparatus, using a cross-linked cyanopropylmethylphenylsilicone capillary column with which impurities of very small amounts can be separated, and with which non-reacted raw materials and by-products, which have a wide range of boiling points can be quantitated. The present invention further provides a process control method of a production method of fluoromethyl-1,1,1,3,3,3 -hexafluoroisopropyl ether, which is characterized in that the content of a particular component in one of the following steps is determined and in that, assuming this as a variable, the treatment condition of the step is adjusted: 1) a step of reacting together 1,1,1,3,3,3 -hexafluoroisopropyl alcohol, (para) formaldehyde, and hydrogen fluoride in the presence of sulfuric acid; 2) a step of contacting a crude fluoromethyl-1,1,1,3,3,3 -hexafluoroisopropyl ether with an alkali aqueous solution and/or water; and 3) a step of distilling crude fluoromethyl-1,1,1,3,3,3 -hexaflouroisopropyl ether
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