HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29144Generated: October 29, 2026
Sodium Hydroxide → Salclobuzate Sodium
https://huagongshe.com/reaction/29144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(4-Chloro-2-hydroxybenzamido)butanoic acid | HCID 9881580 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Salclobuzate Sodium | HCID 23664294 | 92% |
Reaction Steps
A one liter, four neck round bottom flask was equipped with an overhead stirrer, reflux condenser, thermocouple temperature read out, and heating mantle. The following reaction was run under a dry nitrogen atmosphere. Isopropanol (400 mL) and 4-[(4-chloro-2-hydroxy-benzoyl)amino]butanoic acid (25.0 g, 0.09 mol) were charged to the reactor and stirring was started. The reaction slurry was heated to 50° C. until a hazy brown solution was obtained. The warm solution was filtered through a warm pressure filter dressed with Whatman #1 paper into a clean 1 L reactor. The clear yellow filtrate was heated to 62° C. while stirring. Sodium hydroxide solution (50% aqueous; 7.2 g, 0.09 mol) was charged to the reactor while maintaining vigorous agitation. After the base addition was complete, the reactor was heated to reflux (72° C.) and then allowed to cool slowly to ambient temperature. The product was isolated by vacuum filtration through a sintered glass funnel and vacuum dried at 50° C. for 24 hours to give 23.16 g of sodium 4-[(4-chloro-2-hydroxybenzoyl)amino]butanoate as an off-white solid. The yield was 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07420085B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-7387793bf4b847f5ac8d6337a2ba1c53 |
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| Source note | uspto-grants-2008_09 |
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