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filingDate 2002-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1d047b23de993400095ba3811a9117a
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publicationDate 2003-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003018219-A1
titleOfInvention Process for preparation of substituted aromatic compound employing friedel-crafts reaction using a reusable basic anionic clay catalyst
abstract A process for Friedel-Crafts type liquid-phase alkylation or acylation of an aromatic compound using a hydrotalcite-type basic anionic clay catalyst represented by a formula. n [(M 2+ ) 1−x (M 3+ ) x (OH) 2 ] x+ [A y− ] x,y q H 2 O n where M 2+ is a divalent cation selected from Mg 2+ , Zn 2+ , Ni 2+ , Co 2+ , Mn 2+ , Cu 2+ or a mixture thereof, n M 3+ is a trivalent cation selected from Ga 3+ , In 3+ Al 3+ , Fe 3+ Cr 3+ or a mixture thereof; x is a mole fraction of trivalent cations in the range of about 0.05 to about 0.5; O is oxygen; H is hydrogen; A y− is an anion; y minus is an anionic negative charge having a value of 1 minus or 2 minus; and q is a number of water molecules, as the water of hydration; and involving following steps: n i. pretreating said catalyst by contacting it with a halogen containing compound in the presence or absence of a non-aqueous solvent and optionally washing the pretreated catalyst with non-aqueous solvent or liquid aromatic compound to be alkylated or acylated; and then n ii. contacting a liquid reaction mixture comprising said aromatic compound and said alkylating or acylating agent in the presence or absence of a non-aqueous solvent with the catalyst obtained from step (i) in a stirred batch reactor fitted with a reflux condenser under vigorous stirring, in the presence or absence of an inert gas bubbling through the reaction mixture, at effective reaction conditions; n iii. cooling the reaction mixture to a temperature about 30° C., removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture, and optionally washing the used catalyst by non-aqueous solvent;, and if desired, n iv. reusing the used catalyst directly with or without drying for the subsequent reaction batch avoiding step (i), is disclosed.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007232775-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007004588-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6984760-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106631652-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9458128-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7541417-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7449425-B2
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priorityDate 2000-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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