돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662981생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1662981

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 번호US08034810B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-e6d73a7fc56441cc9623d82a9fb4a2c7
출처 메모uspto-grants-2011_10