http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-1816754-C
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c7b40cd57ba8e746481b0dcdbab955d |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-14 |
filingDate | 1990-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1993-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce3a54873cfe42f8eece15eb046cf868 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb17ceed84d1af5cab51f531cb40160d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83f1182e60b24af000fdd5ba42005c42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6073a2fc206c38d6fa6e30da8568fca9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a8350e061b26a61a4d48fbe9726099c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e373e5bb9e17a4b9ec070d8030f2b1c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_833f2356773b2379048cfd09a992ea6a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f237c7569ca1d3cd619a53f5ee0f7b4 |
publicationDate | 1993-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | RU-1816754-C |
titleOfInvention | Method of synthesis of alcohol or phenol difluoromethyl esters |
abstract | Usage: As components of liquid crystal compositions for electro-optical devices. Essence: an improved method for the preparation of difluoromethyl ethers or phenols of the general formula R — OCHPr, where R is lower alkyl, cyclohexyl. Alk - SvNyu - CeHto - CHa, Alk - SvZhO - SvN4CH2. RI - C “Nude. where Ri is Alk. Alk - SvN, R2 - CeN ", where: R2 - CN. Alk, Alk - SeN Alk - CBH4. Afk - SbNu - SvZhO, where Alk - SzNU, CsHn. Reagent 1: chlorodifluoromethane. Reagent 2: corresponding alcohol, Reaction conditions: two-phase system, temperature 20-60 °; C, catalyst: a mixture of quaternary ammonium hydroxide of the formula (8h) OH, where Rs SMz, C4Y9, go and try tritylbenzylammonium with three trimethylbenzylammonium chloride in a molar ratio of alcohol: quaternary ammonium hydroxide or trichloroethyltrimethylthenethyltriethylthenethylthenethylthenethylthenethylthenethylthenethylthenethisethyl : (0.6-1.3): {0.0002-0.002), in an organic solvent. The yield of the target product to 100%. New phycols of iclohexanol are obtained. 1 tab. yo yo |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9150491-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011086933-A1 |
priorityDate | 1990-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 56.