Formic Acid → HCID 13075532, compound
Reaction equation
[I:1][C:2](=[C:5]([I:7])[I:6])[CH2:3][OH:4].[CH:8](O)=[O:9]>>[CH:8]([O:4][CH2:3][C:2]([I:1])=[C:5]([I:7])[I:6])=[O:9]Participants
3
Procedure
2.0 g of 2,3,3-triiodoallyl alcohol and 30 ml of formic acid were refluxed, with stirring, for 3 hours. After cooling the mixture, the crystals which precipitated were collected by filtration, dissolved in ethyl acetate, adsorbed in a dry silica gel chromatography column and eluted with 3:1 by volume mixture of hexane and ethyl acetate, to give 1.8 g of the desired Compound No. 81 in the form of crystals melting at 84°-85° C.
Workup
- temperatureAfter cooling the mixture
- customthe crystals which precipitated
- filtrationwere collected by filtration
- dissolutiondissolved in ethyl acetate
- washeluted with 3:1 by volume mixture of hexane and ethyl acetate
Sources & evidence
- ORD record
- ord-9967c43190c74e3fbd834ca8706d02c5
- Source dataset
- uspto-grants-1984_12
- Patent number
- US04487781
Reaction notes
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