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HRID 6458作成日:2026年10月24日

Water → (4R-cis)-1,1-dimethylethyl 6-(4-nitrobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetate

https://huagongshe.com/ja/reaction/6458

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-Nitrobenzenesulfonyl chlorideHCID 7404—
反応物TriethylamineHCID 8471—
反応物tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonateHCID 9816650—
溶媒DichloromethaneHCID 6344—
生成物(4R-cis)-1,1-dimethylethyl 6-(4-nitrobenzenesulfonyloxymethyl)-2,2-dimethyl-1,3-dioxane-4-acetateHCID 22847683110.5%

反応手順

To a stirring 20°-25° C. solution of the (4R-cis)-1,1-dimethylethyl 6-hydroxymethyl-2,2-dimethyl-1,3- dioxane-4-acetate (European Patent Application 0319,847) (10 g, 0.038 mol) in methylene chloride (250 mL) containing triethylamine (7 mL, 0.05 mol) is added 4-nitrobenzenesulfonyl chloride (10.5 g, 43 mmol). Stirring is continued at 20°-25° C. for 22 hours, the solution is poured onto 200 mL of water and the layers separated. The upper aqueous layer is extracted with 250 mL of methylene chloride and the combined organic layers are washed with 100 mL each of saturated sodium bicarbonate solution to ensure complete removal of 4-nitrobenzenesulfonyl chloride and then saturated sodium chloride solution. Drying the solution with magnesium sulfate and concentration in vacuo gives 18.7 g of the product as a brown oil which solidifies immediately.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248793
出典データセットuspto-grants-1993_09
ORD IDord-a12e310df1644252937b6e4ef4818172
出典メモuspto-grants-1993_09