戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1081646作成日:2026年10月27日

Water → 1-(3-(Phenylmethoxy)phenyl]undecanol

https://huagongshe.com/reaction/1081646

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物UndecanalHCID 8186—
反応物1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-(Phenylmethoxy)phenyl]undecanolHCID 1995546689%

反応条件

温度-70 °C

反応手順

Under a nitrogen atmosphere, a solution of 17.0 grams (0.065 mole) of 3-(phenylmethoxy)phenyl bromide in 125 mL of tetrahydrofuran was stirred and cooled to -70° C. To this was added dropwise 28.0 mL (0.071 mole) of 2.5M n-butyllithium (in hexanes) during a 15 minute period. The reaction mixture temperature was maintained below -60° C. during the addition. Upon completion of addition, a solution of 11.5 grams (0.068 mole) of undecanaldehyde in 15 mL of tetrahydrofuran was added dropwise during a 5 minute period. Upon completion of addition, the reaction mixture was allowed to warm to 0° C. during a one hour period. The reaction mixture was again cooled to -60° C., and 100 mL of water was added. The reaction mixture was allowed to warm to ambient temperature, and then it was extracted with 200 mL of diethyl ether. The ether extract was washed with 50 mL of water, and then it was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel. Elution was accomplished using 9:1 petroleum ether and diethyl ether, and 7:3 petroleum ether and diethyl ether. The product-containing fractions were combined and concentrated under reduced pressure, yielding 20.5 grams of 1-[3-(phenylmethoxy)phenyl]undecanol. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05587379
出典データセットuspto-grants-1996_12
ORD IDord-02e95c0a022441f69d992e90574da569
出典メモuspto-grants-1996_12