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HRID 2581생성일: 2026년 10월 23일

Hydrochloric Acid → 9-Octylheptadecan-9-ol

https://huagongshe.com/ko/reaction/2581

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl CarbonateHCID 7766—
반응물1-BromooctaneHCID 8140—
반응물MagnesiumHCID 5462224—
용매Diethyl EtherHCID 3283—
생성물9-Octylheptadecan-9-olHCID 87239—

반응 조건

온도30 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728907
출처 데이터셋uspto-grants-1998_03
ORD IDord-6e731b1d7e854c2a8e627b73580568d3
출처 메모uspto-grants-1998_03