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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1946생성일: 2026년 10월 24일

Triethylamine → Methanesulfonic Acid

https://huagongshe.com/ko/reaction/1946

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diolHCID 15789229—
용매1,4-DioxaneHCID 31275—
생성물Methanesulfonic AcidHCID 6395—
생성물4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diolHCID 15789229—

반응 단계

Bis(5 -cyclohexyl-4-hydroxy-2-methylphenyl)-3,4-dihydroxyphenylmethane(1.0 mole), naphthoquinone-1,2-diazido-5-sulfonyl chloride (2.0 moles) and methanesulfonyl chloride(0.5 moles) were dissolved in dioxane (4,000 g). To the resulting solution, dioxane (1,500 g) having triethylamine (500 g) dissolved therein was added dropwise over 40 minutes at a controlled temperature not higher than 35° C. The precipitating salt was separated by filtration and the thus recovered reaction product was washed and dried to yield a mixed ester of bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)-3,4-dihydroxyphenylmethane with naphthoquinone-1,2-diazido-5-sulfonic acid and methanesulfonic acid; the average degree of esterification was 50% for the quinonediazidosulfonate ester and 12% for the methanesulfonate ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728504
출처 데이터셋uspto-grants-1998_03
ORD IDord-1a28675e5d044056be5059476c8f3ce9
출처 메모uspto-grants-1998_03