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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 722452생성일: 2026년 10월 24일

Hydrochloric Acid → [(4-Hydroxy-benzenesulfonyl)-(4-methoxy-benzyl)amino]-acetic acid methyl ester

https://huagongshe.com/ko/reaction/722452

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물N-((4-Methoxyphenyl)methyl)glycine methyl esterHCID 10846084—
반응물4-Hydroxybenzene-1-sulfonyl chlorideHCID 11424093—
용매DichloromethaneHCID 6344—
생성물[(4-Hydroxy-benzenesulfonyl)-(4-methoxy-benzyl)amino]-acetic acid methyl esterHCID 67435286—

반응 단계

To a solution of 8.7 g (45.2 mmol) of 4-hydroxybenzenesulfonyl chloride in 80 ml of CH2Cl2, a solution of 6.75 g (32.3 mmol) of (4-methoxy-benzylamino)-acetic acid methyl ester in 20 ml of CH2Cl2 and 12 ml (79.2 mmol) of triethylamine were added dropwise at 0° C. The resulting mixture is stirred for 4 h at r.t., neutralized with cold 1 N aqueous HCl and extracted with CH2Cl2. The combined extracts are washed with H2O and brine, dried over MgSO4 and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel (eluent; AcOEt:CH2Cl2=50:1˜5:1) to give [(4-hydroxy-benzenesulfonyl)-(4-methoxy-benzyl)-amino]-acetic acid methyl ester; NMR (CDCl3): 3.57 (s, 3H), 3.79 (s, 3H), 3.90 (s, 2H), 4.40 (s, 2H), 5.59 (s, 1H), 6.84 (d, 2H, J=8.6 Hz), 6.93 (d, 2H, J=10.64 Hz), 7.15 (d, 2H, J=8.6 Hz), 7.82 (d, 2H, J=10.64 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138432B1
출처 데이터셋uspto-grants-2006_11
ORD IDord-707e94c687d34ed5b96fd3c94e407fc5
출처 메모uspto-grants-2006_11