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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264349Generated: October 26, 2026

Hydrochloric Acid → 4-[4-(Benzenesulfonylamino)-phenyl]-butyric acid

https://huagongshe.com/reaction/1264349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 4-aminobenzenebutanoateHCID 88628—
SolventDichloromethaneHCID 6344—
Product4-[4-(Benzenesulfonylamino)-phenyl]-butyric acidHCID 984003596.7%

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541661B1
Source datasetuspto-grants-2003_04
ORD IDord-c372fef9087f447b9b2ffcc98699279c
Source noteuspto-grants-2003_04