HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 916498Erstellt: 25. Oktober 2026
Hydrochloric Acid → 4-[4-(Benzenesulfonylamino)-phenyl]-butyric acid
https://huagongshe.com/reaction/916498
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | Benzenesulfonyl chloride | HCID 7369 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Methyl 4-aminobenzenebutanoate | HCID 88628 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-[4-(Benzenesulfonylamino)-phenyl]-butyric acid | HCID 9840035 | 96,7% |
Reaktionsschritte
To a solution of 40 (500 mg, 2.59 mmol) in CH2Cl2 at room temperature were added Et3N (901 μL, 6.48 mmol) followed by benzenesulfonyl chloride (661 μL, 5.18 mmol). The mixture was stirred overnight at room temperature then treated with a saturated aqueous solution of NH4Cl. The phases were separated and the organic layer was extracted several times with CH2Cl2. The combined organic extracts were dried over (MgSO4) then evaporated under reduced pressure. The residue was dissolved in a solvent mixture of THF (25 mL) and water (25 mL) then LiOH (1.08 g, 25.9 mmol) was added. The mixture was heated at 50° C. for 1 h then treated with HCl (1N) until pH2. The phases were separated and the aqueous layer was extracted several times with AcOEt. The combined organic extracts were dried over (MgSO4) then evaporated. The crude was purified by flash chromatography using CH2Cl2/MeOH (95:5) as solvent mixture yielding 41 (800 mg, 96%) as a white solid
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | USRE039850E1 |
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| Quelldatensatz | uspto-grants-2007_09 |
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| ORD ID | ord-cb0847c1f65f43d4a9e1ee3acae7bff8 |
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| Quellennotiz | uspto-grants-2007_09 |
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