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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65278생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/65278

반응식

참여 물질

역할이름HCID투입량
반응물BenzophenoneHCID 3102—
반응물5-Tert-butyl-m-xyleneHCID 7378—
반응물ChlorobenzeneHCID 7964—
반응물DiazodimedoneHCID 353445—
촉매MercuryHCID 23931—
생성물2-(2',6'-Dimethyl-4'-t-butylphenyl)-5,5-dimethyl-1,3-cyclohexanedioneHCID 1255633811%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04613617
출처 데이터셋uspto-grants-1986_09
ORD IDord-70011b4f8d694016b0837d15af9bff3c
출처 메모uspto-grants-1986_09