HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374702Generated: October 30, 2026
Hydrochloric Acid → 6-[4-(2-hydroxybenzoylamino)benzoylamino]hexanoic acid
https://huagongshe.com/reaction/2374702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Salicyloyl chloride | HCID 74041 | — |
| Reactant | HCID 23118554 | HCID 23118554 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-[4-(2-hydroxybenzoylamino)benzoylamino]hexanoic acid | HCID 12106175 | — |
Reaction Steps
To a solution of 2.81 g (10.64 mmol) of methyl 6-(4-aminobenzoylamino)hexanoate dissolved in 50 ml of acetonitrile, very slowly add 1.42 g (9.10 mmol) of 2-hydroxybenzoyl chloride dissolved in 5 ml of acetonitrile. Then add 0.92 g (9.10 mmol) of triethylamine and keep the reaction mixture at room temperature for 24 hours. Eliminate the solvent at low pressure, add 30 ml of 10% NaOH to the crude product and continue stirring the mixture until the solid has completely disappeared. Immediately acidify with concentrated hydrochloric acid, filter the resulting solid and wash several times with water. Purify the reaction product by recrystallization (EtOH/H2O). This yields 1.11 g (33%) of 6-[4-(2-hydroxybenzoylamino)benzoylamino]hexanoic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462735B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-50da7151beae4f9a83a56f2128781fe2 |
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| Source note | uspto-grants-2008_12 |
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