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HRID 1946作成日:2026年10月23日

Triethylamine → Methanesulfonic Acid

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diolHCID 15789229—
溶媒1,4-DioxaneHCID 31275—
生成物Methanesulfonic AcidHCID 6395—
生成物4-[Bis(5-cyclohexyl-4-hydroxy-2-methylphenyl)methyl]benzene-1,2-diolHCID 15789229—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728504
出典データセットuspto-grants-1998_03
ORD IDord-1a28675e5d044056be5059476c8f3ce9
出典メモuspto-grants-1998_03