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HRID 22576作成日:2026年10月26日

Acetic Acid → 3-(2,2-Dimethyldihydrobenzofuran-5-yl)-5,7-di-tert-butylbenzofuran-2-one

https://huagongshe.com/reaction/22576

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Methanesulfonic AcidHCID 6395—
反応物2,4-Di-tert-butylphenolHCID 7311—
反応物3-(4-Allyloxyphenyl)-5,7-di-tert-butylbenzofuran-2-oneHCID 19930565—
生成物3-(2,2-Dimethyldihydrobenzofuran-5-yl)-5,7-di-tert-butylbenzofuran-2-oneHCID 7027243020%

反応条件

温度220 °C

反応手順

A mixture of 20.6 g (0.10 mol) of 2,4-di-tert-butylphenol and 22.6 g (0.10 mol) of 4-methallyloxymandelic acid (preparation as in Example 1) is kept at 155° C. under reduced pressure (50 mbar) for 8 hours. The reaction mixture is then heated to 220° C. under nitrogen and kept at this temperature for about 100 minutes. After cooling to about 120° C., 100 ml of acetic acid and 2 ml of methanesulfonic acid are added and the solution is refluxed for 3 hours. The reaction mixture is cooled, and the product is precipitated with 10 ml of ethanol and isolated by filtration. Recrystallisation from ethanol (100 ml)/acetic acid (8 ml) gives 8.0 g (20%) of 3-(2,2-dimethyldihydrobenzofuran-5-yl)-5,7-di-tert-butylbenzofuran-2-one, m.p. 164°-166° C. (compound (102), Table 1 ).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428177
出典データセットuspto-grants-1995_06
ORD IDord-7c22e702c69b48c5a3d0cfb18b638bfb
出典メモuspto-grants-1995_06