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HRID 537598作成日:2026年10月26日

Hydrochloric Acid → 2-Docosyloxy-4-methoxybenzyl alcohol

https://huagongshe.com/reaction/537598

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Potassium CarbonateHCID 11430—
反応物2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
反応物1-BromodocosaneHCID 81355—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
生成物2-Docosyloxy-4-methoxybenzyl alcoholHCID 5325721064.4%

反応条件

温度100 °C

反応手順

2-Hydroxy-4-methoxybenzaldehyde (5 g, 32.9 mmol), 1-bromodocosane (16.6 g, 42.7 mmol) and potassium carbonate (14.8 g, 107 mmol) were mixed with DMF (150 ml), and the mixture was stirred at 100° C. for 7 hr. Chloroform (400 ml) and 1N hydrochloric acid (300 ml) were added to the reaction mixture, and the mixture was washed. The organic layer was washed successively with 1N hydrochloric acid and saturated brine. The organic layer was concentrated and slurry-washed with methanol. The precipitate was collected by filtration and dried under reduced pressure. The obtained dried crystals were dissolved in THF (150 ml), sodium borohydride (3.7 g) was added, and the mixture was stirred at 40° C. for 3 hr. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was concentrated. The mixture was extracted with chloroform, and washed successively with aqueous sodium hydrogen carbonate solution and saturated brine. The organic layer was concentrated. The obtained residue was washed with acetonitrile, and the precipitate was collected by filtration and dried under reduced pressure to give 2-docosyloxy-4-methoxybenzyl alcohol (9.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859732B2
出典データセットuspto-grants-2014_10
ORD IDord-1e8858f487b24899b0dcdb987cbceddc
出典メモuspto-grants-2014_10