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HRID 34289作成日:2026年10月25日

Ammonium Chloride → 1-(1,3-Dioxolan-2-yl)-1,4-epoxy-1,4-dihydronaphthalene

https://huagongshe.com/reaction/34289

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1-Bromo-2-fluorobenzeneHCID 61259—
反応物2-Furyl-1,3-dioxolaneHCID 263158—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物1-(1,3-Dioxolan-2-yl)-1,4-epoxy-1,4-dihydronaphthaleneHCID 1420869577.1%

反応手順

2-Bromofluorobenzene (36.0 g, 0.222M) in THF (200 ml) was added dropwise over one hour to a refluxing mixture of the above furan (28.0 g, 0.200M) and magnesium turnings (5.4 g, 0.206M) in dry THF (200 ml) under nitrogen. After the addition was complete, refluxing was continued for one hour. The cooled mixture was then poured onto saturated NH4Cl solution (250 ml), the organic layer separated and the aqueous layer re-extracted with ether. The combined organic extract was washed with saturated NH4Cl solution, dried over anhydrous K2CO3 -Na2SO4 and concentrated in vacuo. The residue was purified on the Waters Prep 500 HPLC using two columns and eluting with EtOAc/hexane (1:4). A total of 33.3 g of 1-(1,3-dioxolan-2-yl)-1,4-epoxy-1,4-dihydronaphthalene was obtained as a pale yellow oil. Crystallization of the oil from hexane gave 32.5 g (75% yield) as white crystals, mp 48°-49° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04761413
出典データセットuspto-grants-1988_08
ORD IDord-6aa4ee50a8b04b80861eb61277898de3
出典メモuspto-grants-1988_08