HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105956Generated: October 27, 2026
Sodium Acetate → 5-Iodo-2'-methyl salicylanilide
https://huagongshe.com/reaction/1105956
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Hydroxy-5-iodobenzamide | HCID 10563477 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Iodo-2'-methyl salicylanilide | HCID 20555414 | — |
Reaction Steps
37.1 g. of 5-iodo salicylamide, 43.6 g. of 2-methyl benzene, 10 g. of anhydrous sodium acetate, 1 g. of copper bronze are mixed together and heated under reflux for 4 hours. The molten mass obtained is dissolved in alcohol. Said solution is filtered and concentrated by evaporation. 5-iodo-2'-methyl salicylanilide is obtained thereby. Said compound is then dissolved in about 5 times its amount by weight of a mixture of glacial acetic acid and ethyl acetate (1:1). A solution of 40.8 g. of bromine in 30 cc. of glacial acetic acid is added to said solution to obtain 5-iodo-2'-methyl-4'-bromo salicylanilide. Resulting compound (compound No. 5) forms colorless needle-shaped crystals having properties shown in Table 5 by recrystallizing from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04310682 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-bb6bcb440b6c4a8892e05b3366825bdb |
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| Source note | uspto-grants-1982_01 |
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