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HRID 2050993作成日:2026年10月26日

Sodium Chloride → Bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinate

https://huagongshe.com/reaction/2050993

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物tert-Butyl hydroperoxideHCID 6410—
反応物Bis(2,2,6,6-tetramethyl-4-piperidyl) succinateHCID 93340—
触媒Molybdenum trioxideHCID 14802—
溶媒CyclohexaneHCID 8078—
生成物Bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinateHCID 21026400137.6%

反応条件

温度140 °C

反応手順

A two-phase mixture of 70% aqueous tert-butyl hydroperoxide (103.9 grams, 807 mmol), cyclohexane (200 ml) and sodium chloride (15 grams) is shaken in a separatory funnel. The organic phase is dried over anhydrous magnesium sulfate, filtered and added to 40 grms (101 mmol) of bis(2,2,6,6-tetramethylpiperidin-4-yl) succinate. Molybdenum trioxide (2.0 grams) is added and the mixture is heated at reflux for one hour. Water is collected in a Dean-Stark trap. The entire reaction mixture is then transferred to a Fischer-Porter pressure bottle and heated for six hours at 140° C. Additional tert-butyl hydroperoxide (90%, 10.1 grams, 101 mmol) is added and heating is resumed for another four hours. The colorless reaction mixture is filtered, concentrated and dissolved in heptane (200 ml). The heptane solution is passed through a column of silica gel with heptane as the eluent to obtrain 41.2 grams (69% yield) of bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) succinate as a white solid melting at 122-126° C. Further elution of the column with 10:1 heptane:ethyl acetate affords the title compound as a mixture of cyclohexanediyl isomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05015682
出典データセットuspto-grants-1991_05
ORD IDord-42a3961cd5d143c0a582000de5c84ccd
出典メモuspto-grants-1991_05