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HRID 25644作成日:2026年10月25日

p-Toluenesulfonate → HCID 178486035、化合物

https://huagongshe.com/reaction/25644

反応式

関与物質

役割名称HCID仕込み量
反応物p-ToluenesulfonateHCID 85570—
反応物HCID 178486034HCID 178486034—
溶媒MethanolHCID 887—
生成物HCID 178486035HCID 178486035107.3%

反応手順

A solution of 3.45 g (9.44 mmol) of trans-Methyl-{4-[4-(tetrahydro-pyran-2-yloxy)-but-1-ynyl]-cyclohexyl}-carbamic acid tert-butyl ester and 0.7 g (2.83 mmol) of pyrimidium toluene-4-sulfonate in 25 ml MeOH was stirred at 55° C. for 1.5 h. The reaction was partitioned between aqueous solution of 10% KHSO4/ether (3×). The organic phases were washed with aqueous saturated NaHCO3, 10% NaCl, dried over Na2SO4 and evaporated to give 2.85 g (quantitative) of trans-[4-(4-Hydroxy-but-1-ynyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester, MS: 281 (M).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858651B2
出典データセットuspto-grants-2005_02
ORD IDord-3be0d935e22a48a8b35edee8c35950cd
出典メモuspto-grants-2005_02