Benzoic acid, 2,4,6-triiodo- → HCID 21438011, compound
Reaction equation
[I:1][C:2]1[CH:10]=[C:9]([I:11])[CH:8]=[C:7]([I:12])[C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:15])=O>>[I:1][C:2]1[CH:10]=[C:9]([I:11])[CH:8]=[C:7]([I:12])[C:3]=1[C:4]([Cl:15])=[O:5]Participants
3
Procedure
2,4,6-Triiodobenzoic acid (15 g) was suspended in thionyl chloride (75 ml) was refluxed. Thirty minutes after the starting material was dissolved, the reaction solution was cooled and evaporated in vacuo. The residue was dissolved in hot benzene (40 ml), cooled to room temperature, filtered and the filtrate evaporated in vacuo. Yield: 13.6 g. I.R. (KBr): 1785 cm -1 (--COCl).
Workup
- temperaturewas refluxed
- dissolutionThirty minutes after the starting material was dissolved
- temperaturethe reaction solution was cooled
- customevaporated in vacuo
- dissolutionThe residue was dissolved in hot benzene (40 ml)
- filtrationfiltered
- customthe filtrate evaporated in vacuo
Sources & evidence
- ORD record
- ord-a84b296a68a84936a1d4bf1a861bfb06
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04021481
Reaction notes
Loading…