돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726913생성일: 2026년 10월 23일

Acetic Anhydride → 3,7-Di-t-butyldibenziodolium Trifluoromethanesulfonate

https://huagongshe.com/ko/reaction/726913

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물4,4'-Bis(1,1-dimethylethyl)-1,1'-biphenylHCID 74195—
반응물Potassium IodateHCID 23665710—
용매AcetoneHCID 180—
생성물3,7-Di-t-butyldibenziodolium TrifluoromethanesulfonateHCID 867492342%

반응 조건

온도0 °C

반응 단계

Into a 250 ml 3-neck round bottom flask equipped with a mechanical stirrer, thermometer, and inlet was charged with agitation, 4.0 grams (18.8 mmol, 1.0 eq) of potassium iodate, 5.0 grams (18.8 mmol, 1.0 eq) of 4,4'-di-t-butylbiphenyl, and 20 mL of acetic anhydride to form a mixture which was cooled to 0° C. To the mixture was added 5.63 grams (3.32 mL, 37.5 mmol, 2.0 eq) of triflic acid dropwise at such a rate that the reaction temperature did not exceed 10° C. The temperature was kept below 10° C. during the addition by the use of a cooling bath. The reaction mixture was never homogeneous and the 4,4'-di-t-butylbiphenyl did not appear very soluble in the reaction mixture. The reaction mixture turned dark almost immediately upon addition of the triflic acid. The mixture was stirred for about 14 hours at room temperature. The reaction was quenched with approximately 60 mL of water and extracted with methylene chloride. The methylene chloride layer was washed with saturated aqueous sodium bicarbonate solution and concentrated in vacuo. The residue was a dark viscous oil. This material was soluble in ether and could be precipitated with hexanes; however, the precipitate was a brown amorphous powder. Titration with acetone gave a tan solid 0.2 gram (2% yield). Melting point=233°-234° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05710320
출처 데이터셋uspto-grants-1998_01
ORD IDord-9090cb7c2731410ab930c0e7181c744f
출처 메모uspto-grants-1998_01