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HRID 1153719作成日:2026年10月27日

Dichloromethane → 3-(Dodecane-1-sulfonyl)-2-(nitromethylidene)-1,3-thiazinane

https://huagongshe.com/reaction/1153719

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物2-nitromethylenetetrahydro-2H-1,3-thiazineHCID 42853—
反応物Dodecylsulfonyl chlorideHCID 66280—
反応物DiisopropylethylamineHCID 81531—
溶媒WaterHCID 962—
生成物3-(Dodecane-1-sulfonyl)-2-(nitromethylidene)-1,3-thiazinaneHCID 53912032—

反応条件

温度10 °C

反応手順

1.6 g of 2-(nitromethylene)-tetrahydro-2H-1,3-thiazine, 3.18 g of ethyldiisopropylamine and 20 ml of methylene chloride were mixed. The mixture was cooled to and stirred at -60° C. under a nitrogen atmosphere while 2.95 g of dodecanesulfonyl chloride was added in portions over a 10 minute period. The mixture was allowed to warm to 10° C. (2.5 hours), then stirred at 10° C. for 1 hour and at 20° C. for 1.5 hours. The resulting mixture was poured into water, and the organic phase was separated, dried (MgSO4), filtered and stripped of solvent. The residue, a gum, was chromatographed over silica gel, using methylene chloride as eluent. After workup the product was recrystallized from ethanol to give N-(dodecylsulfonyl)-2-(nitromethylene)-tetrahydro-2H-1,3-thiazine (3A) as a solid, m.p.: 116°-117° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04486427
出典データセットuspto-grants-1984_12
ORD IDord-b1afed8fd099419786edb1cc6b2f27d9
出典メモuspto-grants-1984_12