Sodium Bisulfite → HCID 86743919, compound
Reaction equation
[F:1][C:2]([F:21])([F:20])[C:3]([NH:5][C:6](=[C:8]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:9]([O:11]CC)=[O:10])[CH3:7])=[O:4].S(=O)(O)[O-].[Na+]>[I-].C[SiH](C)C>[F:1][C:2]([F:20])([F:21])[C:3]([NH:5][C:6](=[C:8]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:9]([OH:11])=[O:10])[CH3:7])=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
16.5 g of the product of Step A were dissolved in 15.6 ml of trimethylsilane iodide and after 16 hours of reflux, the solution was poured into 200 ml of a solution of sodium bisulfite and then was extracted with ether. The extracts were washed with water, dried and concentrated to dryness under reduced pressure to obtain 11.7 g of the expected product which after crystallization from heptane melted at 174° C.
Workup
- temperatureof reflux
- extractionwas extracted with ether
- washThe extracts were washed with water
- customdried
- concentrationconcentrated to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-1af07898159646108e3257483765527c
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04987140
Reaction notes
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