HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chlorosalicylic Acid → HCID 929387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chlorosalicylic Acid | HCID 9447 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 929387 | HCID 929387 | — |
Reaction Steps
For example, a mixture of a compound of formula 40 wherein R3 and R4 are hydrogen and R5 is chloro, i.e., 5-chloro-2-hydroxy benzoic acid, (5.0 g, 29 mmol) and N-iodosuccinimide (7.17 g, 32 mmol) in acetic acid (30 mL) was heated to 95° C. for 2 h. Additional N-iodosuccinimide (0.70 g, 3.1 mmol) was added and heating was continued for 1 h. The mixture was cooled and poured over ice. The precipitate was isolated by filtration and the crude material was purified by recrystallization from methanol/water. The solid was isolated by filtration, rinsed with water and dried. 5-Chloro-2-hydroxy-3-iodo-benzoic acid 41 was obtained as a tan crystalline solid (6.14 g, 71% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867200B1 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-093588158f1a480cb2455fe4b72ca58d |
| Source note | uspto-grants-2005_03 |