Dichloromethane → HCID 380419, compound
Reaction equation
[CH2:1]1[S:9](=[O:11])(=[O:10])[O:8][CH2:7][CH2:6][O:5][S:2]1(=[O:4])=[O:3].[H-].[Na+].C1C=CC(S(N(S(C2C=CC=CC=2)(=O)=O)[F:24])(=O)=O)=CC=1.C(Cl)Cl>C1COCC1.CC#N.C1CCCCC1>[F:24][CH:1]1[S:2](=[O:3])(=[O:4])[O:5][CH2:6][CH2:7][O:8][S:9]1(=[O:11])=[O:10]Participants
8
Procedure
To a solution of 2.4 g of ethylene methanedisulfonate in 20 mL of THF and 0.35 g of NaH was added 3.8 g of N-fluorobenzene sulfonimide in 25 mL of CH3CN. The product was isolated by crystallization from CH2Cl2 and cyclohexane to give 0.4 g of ethylene fluoromethane disulfonate which was brominated in H2O to give ethylene fluorobromomethanedisulfonate, m.p. 82-90° C. (93-3).
Sources & evidence
- ORD record
- ord-f75b0f44aa064d5abe0be21fdf0cc7b8
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08124793B2
Reaction notes
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