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HRID 596887作成日:2026年10月26日

Hydroquinone → 1,3-Bis(Hydroxymethyl) Benzene Bis (2-Cyanoacrylate)

https://huagongshe.com/reaction/596887

反応式

関与物質

役割名称HCID仕込み量
反応物HydroquinoneHCID 785—
反応物Maleic AnhydrideHCID 7923—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物1,3-BenzenedimethanolHCID 69374—
反応物HCID 21226398HCID 21226398—
溶媒O-XyleneHCID 7237—
生成物1,3-Bis(Hydroxymethyl) Benzene Bis (2-Cyanoacrylate)HCID 86734548—

反応手順

A mixture consisting of 30.0 g (0.0474 mole) bisanthracene adduct/1,3-bis (hydroxymethyl) benzene bits (2-cyanoacrylate), 27.8 g (0.284 mole) maleic anhydride, 0.1 g hydroquinone, and 0.5 g phosphorous pentoxide in 125 ml. dry xylene is heated at 139°-141° C for 5 hours, cooled to room temperature, and suction-filled to give 26.1 g, mp 257°-259° C, of A/MA adduct. Solvent stripping of the filtrate and crystallization of the residue from benzene gives another 3.5 g, mp 258°-260° C, of A/MA adduct. The mother liquor is solvent stripped and the excess maleic anhydride sublimed off at 60°-65° C/0.1-0.2mm. The semi-crystalline residue (11.4g) is taken-up in 50 ml. hot benzene, the solution decanted from some insolubles (3.5 g, mp>300° C) and cooled to give another 1.3 g, mp 260°-262° C, of A/MA adduct. The filtrate is concentrated in vacuo to give 6.2 g (44% theory) of crude monomer as a pale orange liquid. IR and NMR analysis indicated the presence of considerable anhydride-containing and other unknown impurities.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04012402
出典データセットuspto-grants-1977_03
ORD IDord-b1bcacf03dce421c9efb06cf7c96c427
出典メモuspto-grants-1977_03