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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 722453생성일: 2026년 10월 25일

1-Bromo-4-fluorobutane → HCID 67436058, 화합물

https://huagongshe.com/reaction/722453

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-4-fluorobutaneHCID 10022—
반응물Potassium CarbonateHCID 11430—
반응물[(4-Hydroxy-benzenesulfonyl)-(4-methoxy-benzyl)amino]-acetic acid methyl esterHCID 67435286—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 67436058HCID 67436058—

반응 단계

To a suspension of 1 g (2.74 mmol) of [(4-hydroxy-benzenesulfonyl)-(4-methoxy-benzyl)-amino]-acetic acid methyl ester and 1.14 g (8.22 mmol) of K2CO3 in 8 ml of DMF, 0.59 ml (5.47 mmol) of 1-bromo-4-fluorobutane is added dropwise at r.t. After stirring for 18 h at r.t., the reaction mixture is diluted with H2O and extracted with AcOEt. The combined extracts are washed with brine, dried over MgSO4 and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel (AcOEt:n-hexane=3:1) to give {[4-(4-fluorobutoxy)-benzenesulfonyl](4-methoxy-benzyl)-amino}-acetic acid methyl ester; NMR (CDCl3): 1.86–1.96 (m, 4H), 3.57 (s, 3H), 3.79 (s, 3H), 3.90 (s, 2H), 4.08 (t, 2H, J=6.04 Hz), 4.39 (s, 2H), 4.46 (t, 1H, J=6.04 Hz), 4.55–4.65 (m, 1H), 6.83 (d, 2H, J=8.56 Hz), 6.97 (d, 2H, J=9.08 Hz), 7.15 (d, 2H, J=8.56 Hz), 7.82 (d, 2H, J=9.08 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138432B1
출처 데이터셋uspto-grants-2006_11
ORD IDord-2959c3dce4c74f8d98c59b7756349ab2
출처 메모uspto-grants-2006_11