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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1919232생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1919232

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium HydroxideHCID 3939—
반응물Benzenesulfonyl chlorideHCID 7369—
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Methyl 4-aminobenzenebutanoateHCID 88628—
용매DichloromethaneHCID 6344—
생성물4-[4-(Benzenesulfonylamino)-phenyl]-butyric acidHCID 984003596.7%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE043343E1
출처 데이터셋uspto-grants-2012_05
ORD IDord-d067cecd5a264c5a93ff09b10a778ee4
출처 메모uspto-grants-2012_05