돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 596887생성일: 2026년 10월 24일

Hydroquinone → HCID 86734548, 화합물

https://huagongshe.com/ko/reaction/596887

반응식

참여 물질

역할이름HCID투입량
반응물HydroquinoneHCID 785—
반응물Maleic AnhydrideHCID 7923—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물1,3-BenzenedimethanolHCID 69374—
반응물HCID 21226398HCID 21226398—
용매O-XyleneHCID 7237—
생성물HCID 86734548HCID 86734548—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04012402
출처 데이터셋uspto-grants-1977_03
ORD IDord-b1bcacf03dce421c9efb06cf7c96c427
출처 메모uspto-grants-1977_03