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HRID 1377227作成日:2026年10月27日

2-(Phenylmethylene)octanal → 1,3-Diphenyl-2-n-hexyl-2-propen-1-ol

https://huagongshe.com/reaction/1377227

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Phenylmethylene)octanalHCID 7585—
反応物MagnesiumHCID 5462224—
反応物Benzene bromideHCID 22259850—
溶媒TetrahydrofuranHCID 8028—
生成物1,3-Diphenyl-2-n-hexyl-2-propen-1-olHCID 53941136115.2%

反応手順

In a 2-liter three-necked flask equipped with a stirring device, a thermometer and a nitrogen substituting device, 13.2 g of magnesium and 300 milliliters of tetrahydrofuran were introduced and stirred violently. Then, a solution of 83.2 g of benzene bromide in 100 milliliters of tetrahydrofuran was added dropwise for 40 minutes. At that time, cooling was carried out with an ice bath if required. After the dropwise addition was ended, stirring was carried out at room temperature for 1 hour, and thereafter 108.2 g of α-n-hexyl cinnamaldehyde was added dropwise. After stirring for one day and one night, the solution was poured in ice water containing dilute hydrochloric acid, and extracted with 1 liter of ethyl acetate. After the solution was washed with an aqueous solution of sodium hydrogencarbonate and water, it was dried with anhydrous magnesium sulfate. After removing the solvent off by a rotary evaporator, 169.6 g of 1,3-diphenyl-2-n-hexyl-2-propen-1-ol was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05663440
出典データセットuspto-grants-1997_09
ORD IDord-cf43499f97234150b816bd638d1d0805
出典メモuspto-grants-1997_09