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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127551생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/127551

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 0.25 N NaOH, washed with ether, acidified with 1 N 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 ractions 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 224°-49° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256657
출처 데이터셋uspto-grants-1981_03
ORD IDord-f865d0a0bb5045e6be6e3838ea1d8289
출처 메모uspto-grants-1981_03