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HRID 1383696作成日:2026年10月27日

Water → 1,3-Cyclopentadiene, octyl-

https://huagongshe.com/reaction/1383696

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl EtherHCID 3283—
反応物1-BromooctaneHCID 8140—
反応物Sodium, 2,4-cyclopentadien-1-yl-HCID 78681—
溶媒TetrahydrofuranHCID 8028—
生成物1,3-Cyclopentadiene, octyl-HCID 52817079%

反応手順

Under a high purity nitrogen atmosphere, 5.8 ml (30 mmol) of 1-bromooctane was introduced into a Schlenck flask and 50 ml of tetrahydrofuran (THF) was added thereto. To the resulting mixture, 18 ml of 2N sodium cyclopentadienide in THF was added at 0° C. The resultant was stirred for 5 hours at room temperature, 100 ml of water and 100 ml of diethyl ether were added thereto, followed by agitation. The diethyl ether layer was dried over anhydrous magnesium sulfate. After filtering magnesium sulfate, the organic solvent was distilled off under a reduced pressure and the residue was subjected to silica gel column chromatography (eluent:hexane) to obtain 4.21 g of n-octylcyclopentadiene (yield: 79%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06255417B1
出典データセットuspto-grants-2001_07
ORD IDord-d425dc7d3c004fe48575805f4eb968c1
出典メモuspto-grants-2001_07