Tetrahydrofuran → HCID 86745982, 화합물
반응식
[Cl-].[Cl-].[Cl-].[Al+3:4].[O:5]1[CH2:9][CH2:8][CH2:7][CH2:6]1.[F:10][Sb-:11]([F:16])([F:15])([F:14])([F:13])[F:12].C([O+](CC)CC)C>C(OCC)C>[F:10][Sb-:11]([F:16])([F:15])([F:14])([F:13])[F:12].[Al+3:4].[O:5]1[CH2:9][CH2:8][CH2:7][CH2:6]1.[F:10][Sb-:11]([F:16])([F:15])([F:14])([F:13])[F:12].[F:10][Sb-:11]([F:16])([F:15])([F:14])([F:13])[F:12]참가 물질
5
실험 절차
0.13 g (0.87 mmol) of aluminium trichloride is dissolved in 2 g of dry diethyl ether, and 5 ml of dry tetrahydrofuran are then added. 10 g (2.95 mmol) of solid triethyloxonium hexafluoroantimonate are added to the clear solution under argon as an inert gas and dissolve immediately. After 5 minutes, the product starts to crystallize out. After 2 hours at 40° C., the product is filtered off under an inert gas, washed twice with dry THF and dried at room temperature under a high vacuum. 0.9 g of fine colourless crystals is obtained.
후처리
- dissolutiondissolve immediately
- customto crystallize out
- waitAfter 2 hours at 40° C.
- filtrationthe product is filtered off under an inert gas
- washwashed twice with dry THF
- customdried at room temperature under a high vacuum
출처 및 근거
- ORD 기록
- ord-2cebcabae464440da8b5a962da98ae85
- 출처 데이터셋
- uspto-grants-1993_01
- 특허 번호
- US05179179
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