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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359899Generated: November 2, 2026

Hydrogen Bromide → HCID 23009947, compound

https://huagongshe.com/reaction/1359899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantEthylene carbonateHCID 7303—
ReactantMethylparabenHCID 7456—
ProductHCID 23009947HCID 23009947—

Reaction Steps

The composition below was prepared, filtered through a polypropylene filter having a pore size of 0.2 μm, and the filtrate was used as coating liquids LC-2 for forming the optically anisotropic layer. LC-2-1 was synthesized according to a method described in Japanese Laid-Open Patent Publication “Tokkaihei” No. 2001-166147. LC-2-2 was synthesized by, dissolving a commercial hydroxyethyl methacrylate, acrylic acid, and M5610 (product of Daikin Industries, Ltd.) in a ratio by weight of 15/5/80 into methyl ethyl ketone (concentration 40%), and the mixture was allowed to polymerize using V-601 (product of Wako Pure Chemical Industries, Ltd.) as a polymerization initiator. LC-2-3 was synthesized by first introducing octyloxybenzoic acid (product of Kanto Chemical Co., Inc.) into an excessive hydroquinone (product of Wako Pure Chemical Industries, Ltd.) based on the mixed acid anhydride process so as to obtain monoacyl phenol compound. Next, methyl p-hydroxybenzoate was converted to a hydroxyl ethyl compound using ethylene carbonate, the resultant ester is hydrolyzed, and brominated with hydrobromic acid to obtain 2-bromoethyloxybenzoic acid. Two these compounds were then esterified by the mixed acid anhydride process to obtain a diester compound, and the product was then converted to a quaternary compound using dimethylaminopyridine, to thereby obtain LC-2-3 as an onium salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879634B2
Source datasetuspto-grants-2011_02
ORD IDord-44f54918372e4c7d815bf599005fa5bc
Source noteuspto-grants-2011_02