Disclosed herein is a process for chemically synthesizing of hydroquinone derivatives, especially for hydroquinone derivatives with heptadecatrienyl side chain, which is synthesized via a Wittig reaction of 2-(10-oxononyl)-1,4-diacetoxyl benzene and (3E, 5Z)-3,5-heptadien-1-triphenylphosphonium iodide and then deacetylation. In addition, the product is solid powder.

The disclosure provides processes for synthesizing compounds for use as CFTR modulators.

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The disclosure provides processes for synthesizing compounds for use as CFTR modulators.

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The present invention relates to a liquid crystal compound having a structure as shown by formula I, wherein R is selected from H and alkyl or alkoxy containing 1-12 carbon atoms in which one or more H are unsubstituted or substituted with halogens; A.sub.1, A.sub.2 and A.sub.3 are each independently selected from: a single bond, 1,4-cyclohexylene, 1,4-phenylene, wherein hydrogen in 1,4-phenylene may be each independently substituted with one or more halogens; and Z.sub.1 and Z.sub.2 are each independently selected from a single bond or (CH.sub.2).sub.2. The compound of the invention has the characteristics of low rotational viscosity, large dielectric anisotropy, good mutual solubility and stability. The driving voltage of a device can be remarkably reduced after the compound is added to a composition. Thus, the compound of the invention has prosperous applications in LCD industry. ##STR00001##

The invention is directed to a process for the preparation of an aromatic acid or a phenolic compound, said process comprising reacting a dienophile and a furanic compound comprising an acetal moiety in a Diels-Alders reaction to obtain an aromatic compound comprising said acetal moiety, followed by hydrolysis and oxidation of said acetal moiety into a hydroxide or carboxylate moiety to form the aromatic acid or phenolic compound, wherein said dienophile is selected from the group consisting of alkylenes, acetylenes, acrylates, maleates, fumarates, maleimides, propiolates, acetylene dicarboxylates, and benzynes and wherein said acetal moiety is bound directly to the 2-position of the furanic compound.

A method of deconstructing polymer waste into at least one useful breakdown product, wherein the polymer waste contains at least one condensation polymer, the method comprising contacting the polymer waste with a catalyst comprising an organic nitrogen-containing base and a carboxylic acid or ester thereof, in the presence of a protic molecule selected from alcohols, diols, polyols, and amines, at an elevated temperature effective for inducing alcoholysis or aminolysis of the condensation polymer, wherein the useful breakdown products comprise monomer species capable of being polymerized, and the organic nitrogen-containing base has the following structure:

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wherein: R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, and R.sup.6 are independently selected from hydrogen atom, electron pair, and alkyl groups containing one to three carbon atoms, and wherein any adjacent two of R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, and R.sup.6 may optionally interconnect to form a five, six, or seven-membered ring.

A method of deconstructing polymer waste into at least one useful breakdown product, wherein the polymer waste contains at least one condensation polymer, the method comprising contacting the polymer waste with a catalyst comprising an organic nitrogen-containing base and a carboxylic acid or ester thereof, in the presence of a protic molecule selected from alcohols, diols, polyols, and amines, at an elevated temperature effective for inducing alcoholysis or aminolysis of the condensation polymer, wherein the useful breakdown products comprise monomer species capable of being polymerized, and the organic nitrogen-containing base has the following structure:

##STR00001##

wherein: R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, and R.sup.6 are independently selected from hydrogen atom, electron pair, and alkyl groups containing one to three carbon atoms, and wherein any adjacent two of R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, and R.sup.6 may optionally interconnect to form a five, six, or seven-membered ring.

The disclosure provides processes for synthesizing compounds for use as CFTR modulators.

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The disclosure provides processes for synthesizing compounds for use as CFTR modulators.

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A macromolecules containing metal and a use thereof as a catalyst, said macromolecules containing metal being obtained by causing a ligand to react with a zinc compound or a cobalt compound, said ligand having an imidazole group that is bonded to a macromolecule via a linker.