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HRID 970942作成日:2026年10月25日

Hydrochloric Acid → HCID 86610996、化合物

https://huagongshe.com/reaction/970942

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TetrahydrofuranHCID 8028—
反応物4-Penten-1-one, 1-(2-naphthalenyl)-HCID 11241273—
反応物HCID 178478988HCID 178478988—
溶媒WaterHCID 962—
生成物HCID 86610996HCID 86610996—

反応手順

First, 6-(2-naphthyl)-6-(3-butenyl)fulvene was prepared from cyclopentadienyl Grignard reagents as follows. A 1 L round bottomed flask was charged with 1-(2-naphthyl)-4-penten-1-one, 97% (21.73 g, 100 mmol), THF (100 mL), and a stir bar, and cooled in an ice bath. Cyclopentadienyl magnesium chloride (150 mL of approximately 1 M solution in THF, 330 mmol) was added dropwise over ½ hour. The yellow solution was stirred for 2 hours in the ice bath. The yellow solution was then refluxed for 2.5 hours, during which time a red color developed. The solution was acidified by first adding 100 mLs of water, and then adding 100 mL of 1 M HCl. The product was extracted with pentane, and the pentane extracts were collected, washed with water, and dried over sodium sulfate. Elution through silica with pentane and concentration under vacuum afforded 20.25 g (73%) of the product 6-(2-naphthyl)-6-(3-butenyl)fulvene as a red oil, which was 93% pure. The major impurity was dicyclopentadiene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312283B2
出典データセットuspto-grants-2007_12
ORD IDord-8ab306f781d844f5bc89967bb4fb4c7a
出典メモuspto-grants-2007_12