HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-fluoro-3-iodo-1H-indole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-fluoro-1H-indole-5-carboxylic acid | HCID 11492033 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-fluoro-3-iodo-1H-indole-5-carboxylic acid | HCID 68328451 | 92% |
Reaction Steps
To a solution of 6-fluoro-1H-indole-5-carboxylic acid (2.32 g, 12.95 mmol) in DMF (15 mL) was added iodine (3.45 g, 13.60 mmol) and potassium hydroxide (1.60 g, 28.5 mmol). After stirring 20 min at RT, the reaction mixture was poured into ice water (40 mL) containing sodium hydrogensulfite (1.35 g, 12.95 mmol). The reaction mixture was stirred for 5 min, treated with 2 N HCl to adjust the pH to about pH=6 and filtered. The resulting orange solid was washed with water (2×25 mL) and transferred to a 250 mL round bottomed flask and dried overnight using a lyophilizer to afford 6-fluoro-3-iodo-1H-indole-5-carboxylic acid (3.63 g, 11.90 mmol, 92% yield) as an orange amorphous solid. MS (ESI, pos. ion) m/z: 305.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321756B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-dc92b6bc798e429c83e97dd62e7ae7fd |
| Source note | uspto-grants-2016_04 |