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HRID 1415571作成日:2026年10月27日

2,5-Di-tert-butylhydroquinone → 3a,4,7,7a-Tetrahydro-1H-4,7-methanoindene-1,3(2H)-dione

https://huagongshe.com/reaction/1415571

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-Di-tert-butylhydroquinoneHCID 2374—
反応物CyclopentadieneHCID 7612—
反応物2-Cyclopentene-1,4-dioneHCID 70258—
溶媒BenzeneHCID 241—
生成物3a,4,7,7a-Tetrahydro-1H-4,7-methanoindene-1,3(2H)-dioneHCID 13587181—

反応手順

A solution of 4-cyclopentene-1,3-dione (5 84g; 0.06 mole) in anhydrous benzene (20ml) was treated with freshly distilled cyclopentadiene (7.3g; 0.122 mole) together with a few crystals of 2,5-di-t-butyl hydroquinone. An immediate reaction ensued with concommitant crystallisation of the product. After standing at room temperature for 3 days the title compound was filtered and recrystallised from methanol, m.p. 183° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04005219
出典データセットuspto-grants-1977_01
ORD IDord-94edf95b6b2e4bf6a0e10601c5ca5b63
出典メモuspto-grants-1977_01