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HRID 2582作成日:2026年10月23日

Hydrochloric Acid → Tri-n-octylmethylmethane

https://huagongshe.com/ja/reaction/2582

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物9-Octylheptadecan-9-olHCID 87239—
反応物Calcium ChlorideHCID 5284359—
反応物TrimethylaluminumHCID 16682925—
反応物Tri-n-octylmethylchlorideHCID 19690384—
溶媒DichloromethaneHCID 6344—
生成物Tri-n-octylmethylmethaneHCID 19690391—

反応条件

温度0 °C

反応手順

This compound may be prepared in the following manner. Three moles of 1-bromooctane are slowly added to 3 moles of magnesium turnings in 0.6 liters of anhydrous ethyl ether (nitrogen atmosphere). One mole of diethyl carbonate in 0.151 anhydrous ethyl ether is slowly added to the mixture. The mixture is stirred for one hour at 30° C., then the mixture is slowly poured into 1.8 liters of a cold 10% HCl solution. The organic layer is dried with magnesium sulfate and the ethyl ether is evaporated off to give tri-n-octylcarbinol. One mole of tri-n-octylcarbinol is added to a mixture of 0.2 liters of methylene chloride and 0.32 moles calcium chloride. Approximately 1.5 moles of HCl gas is slowly bubbled through the solution. The product mixture is then washed with 1 liter of a 10% sodium carbonate solution. The organic layer is dried with magnesium sulfate and the methylene chloride is evaporated off. One mole of tri-n-octylmethylchloride is added to 0.75 liters of methylene chloride and the solution is blanketed with nitrogen and is cooled to 0° C. 0.33 moles of trimethylaluminum is then added and the mixture is allowed to warm to room temperature. The mixture is slowly quenched with 50 ml of water followed by washing with 1 liter of a 10% HCl solution. The organic layer is dried with magnesium sulfate and the solvent is evaporated to give tri-n-octylmethylmethane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728907
出典データセットuspto-grants-1998_03
ORD IDord-b0a83914dba048c6a657be3218f2bd5a
出典メモuspto-grants-1998_03