HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234292Generated: October 29, 2026
Hydrochloric Acid → HCID 178431739, compound
https://huagongshe.com/reaction/234292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 43131892 | HCID 43131892 | — |
| Product | HCID 178431739 | HCID 178431739 | — |
Reaction Steps
A mixture of 5-chloroisatin acetamide (IV, 5.00 g), potassium hydroxide (1N, 56 ml) and THF (18 ml) is heated at reflux for 1 hr, allowing the THF to boil off, and is allowed to cool to 20°-25°. The basic mixture is cooled to 0° and acidified to pH 5.5 (pH paper) with hydrochloric acid (4N). The resulting solids are filtered, washed with water and methylene chloride, dried, and triturated overnight in methylene chloride (200 ml, to remove a small amount of 5-chloroisatin byproduct). These solids are filtered, washed with methylene chloride, and dried to give 6-chloro-2-hydroxyquinoline-4-carboxylic acid (V), mp >300°; IR (mineral oil) 1711, 1645, 1430, 1221,1179, 887 and 881 cm-1 ; NMR (d6 -DMSO) 12.25,8.30, 7.62, 7.38 and 7.00 δ; MS (El, m/e) 223, 178 and 151.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594140 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-0ae0b92d7fda4257a6444402c92d638f |
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| Source note | uspto-grants-1997_01 |
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