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HRID 39409作成日:2026年10月24日

1,2,3-Tribromobenzene → 5-Bromo-9-isopropylidene-1,4-dihydro-1,4-methano-naphthalene

https://huagongshe.com/ja/reaction/39409

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3-TribromobenzeneHCID 11842—
反応物Ammonium ChlorideHCID 25517—
反応物1,3-Cyclopentadiene, 5-(1-methylethylidene)-HCID 137467—
反応物ButyllithiumHCID 178418339—
溶媒TolueneHCID 1140—
生成物5-Bromo-9-isopropylidene-1,4-dihydro-1,4-methano-naphthaleneHCID 5785760566%

反応手順

To a stirred solution of 1,2,3-tribromo-benzene (4.34 g, 13.8 mmol) and 6,6-dimethylfulvene (2.38 g, assay 92.6%, 20.7 mmol) in dry toluene (60 ml) under a nitrogen atmosphere, 5.5 ml of a 2.5M toluene solution of n-butyllithium (14.5 mmol) were added dropwise at −5 to 0° C. within 10 minutes. After a further 10 minutes at 0° C. and 2 hours at ambient temperature, the reaction mixture was poured onto a saturated aqueous solution of ammonium chloride, extracted with ethyl acetate, washed with brine and water, dried over sodium sulphate and evaporated. Purification of the crude material on silca gel in hexane afforded 2.38 g of the desired product as a yellow oil (assay 84% by g.l.c., 55% yield). This reaction is also disclosed in WO 2007/068417.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524915B2
出典データセットuspto-grants-2013_09
ORD IDord-bc797f142524417b8cd33e6edb8dedf8
出典メモuspto-grants-2013_09