Chloroiodomethane → HCID 22035697, 화합물
반응식
[CH3:1][O:2][C:3]1[CH:19]=[CH:18][C:6]([CH2:7][O:8][C:9]2[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.[OH-].C([N+](CCCC)(CCCC)CCCC)CCC.I[CH2:39][Cl:40]>O1CCOCC1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][O:8][C:9]2[CH:17]=[CH:16][C:12]([C:13]([O:15][CH2:39][Cl:40])=[O:14])=[CH:11][CH:10]=2)=[CH:18][CH:19]=1참가 물질
실험 절차
To a solution of 4-(4-methoxybenzyloxy)benzoic acid (5.16 g, 20 mmole) in 100 ml 1,4-dioxane was added a 40% solution of tetrabutylammonium hydroxide (14.27 g, 22 mmole) and the mixture was stirred 2 hours at room temperature. The mixture was evaporated under reduced pressure and co-evaporated two times with 1,4-dioxane and two times with toluene. The dried product was dissolved in 60 ml dichloromethane and iodochloromethane (35.3 g 200 mmole) was added. The solution was stirred for two days at room temperature and evaporated under reduced pressure. About 100 ml ethyl actate was added and the organic phase washed twice with water, dried with sodium sulfate and evaporated under reduced pressure. The product was isolated by silica gel column chrornatography. Yield: 4.48 g=73%
후처리
- customThe mixture was evaporated under reduced pressure
- dissolutionThe dried product was dissolved in 60 ml dichloromethane
- stirringThe solution was stirred for two days at room temperature
- customevaporated under reduced pressure
- additionAbout 100 ml ethyl actate was added
- washthe organic phase washed twice with water
- dry with materialdried with sodium sulfate
- customevaporated under reduced pressure
- customThe product was isolated by silica gel column chrornatography
출처 및 근거
- ORD 기록
- ord-a07f7183f8f749f598f2e192e07868e0
- 출처 데이터셋
- uspto-grants-2002_10
- 특허 번호
- US06458772B1
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