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HRID 264363생성일: 2026년 10월 26일

Ozone → (RS)-2-(2-oxoethyl)-3,3,6-trimethyl-1-indanone

https://huagongshe.com/reaction/264363

반응식

참여 물질

역할이름HCID투입량
반응물OzoneHCID 24823—
반응물(RS)-2-(2-buten-1-yl)-3,3,6-trimethyl-1-indanoneHCID 53745382—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물(RS)-2-(2-oxoethyl)-3,3,6-trimethyl-1-indanoneHCID 1063250894%

반응 단계

An ozone stream (2.5 g ozone/hour) was conducted for 60 minutes while stirring through a solution, cooled to -70° of 12.7 g (RS)-2-(2-buten-1-yl)-3,3,6-trimethyl-1-indanone in 200 ml of anhydrous dichloromethane and 40 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 6.12 ml of dimethyl sulfide, the mixture was stirred at room temperature for 18 hours. The reaction mixture was evaporated in a vacuum, the residue was treated with 150 ml of dichloromethane and, after the addition of 25 ml of water and 25 ml of trifluoroacetic acid, stirred at room temperature for 2.5 hours. The mixture was subsequently poured into 150 ml of water and neutralized by the spatula-wise addition of sodium hydrogen carbonate while stirring. An additional 100 ml of water were added. The phases were separated and the aqueous phase was extracted twice with 150 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. 11.3 g (94%) of (RS)-2-(2-oxoethyl)-3,3,6-trimethyl-1-indanone were obtained as a light yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646173
출처 데이터셋uspto-grants-1997_07
ORD IDord-1ae2dccc4c314ed1a20ba181c62f8de1
출처 메모uspto-grants-1997_07