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HRID 65278作成日:2026年10月26日

Benzophenone → 2-(2',6'-Dimethyl-4'-t-butylphenyl)-5,5-dimethyl-1,3-cyclohexanedione

https://huagongshe.com/reaction/65278

反応式

関与物質

役割名称HCID仕込み量
反応物BenzophenoneHCID 3102—
反応物5-Tert-butyl-m-xyleneHCID 7378—
反応物ChlorobenzeneHCID 7964—
反応物DiazodimedoneHCID 353445—
触媒MercuryHCID 23931—
生成物2-(2',6'-Dimethyl-4'-t-butylphenyl)-5,5-dimethyl-1,3-cyclohexanedioneHCID 1255633811%

反応手順

A solution of 7.00 g (0.042 mol) of 2-diazo-5,5-dimethylcyclohexane-1,3-dione in 300 ml of 5-t-butyl-m-xylene and 250 ml chlorobenzene containing 38.38 g (0.21 mol) of benzophenone was irradiated overnight with a 200 watt mercury arc lamp fitted with a borosilicate glass filter after degassing for 1 hour under nitrogen. The photolysis mixture was extracted with 0.25N NaOH, washed with ether, acidified with 1N HCl, and extracted with chloroform. The chloroform was dried over anhydrous MgSO4 and stripped to give a crude yellow solid. The photolysis was repeated and the combined crude product from these reactions was chromatographed through silica gel (0.063-0.2 mm) using benzene-ethyl acetate. The solid obtained from the chromatography was recrystallized from benzene to give 2.76 g (11%) of 2-(2',6'-dimethyl-4'-t-butylphenyl)-5,5-dimethyl-1,3-cyclohexanedione as white crystals, mp 244°-49° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04613617
出典データセットuspto-grants-1986_09
ORD IDord-70011b4f8d694016b0837d15af9bff3c
出典メモuspto-grants-1986_09