돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2117675생성일: 2026년 10월 25일

Methane → Benzenesulfonamide, 3-[4-[(6-bromohexyl)oxy]butyl]-

https://huagongshe.com/reaction/2117675

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamideHCID 21895558—
생성물Benzenesulfonamide, 3-[4-[(6-bromohexyl)oxy]butyl]-HCID 2189543878.8%

반응 조건

온도20 °C

반응 단계

3-{4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamide (627 g) in IMS (1900 ml) was stirred with activated charcoal (314 g) at room temperature for 2 h and then filtered through a short pad of Celite. The filter pad was washed with IMS (4300 ml) and the filtrate transferred to a hydrogenation vessel. 5% Platinum on Charcoal (520.1 g, 50% water) was added and the reaction mixture was then stirred under an atmosphere of hydrogen (0.2 bar) at 20° C. for 6 h. The mixture was then filtered through a short pad of Celite and concentrated under reduced pressure to give the title compound (499 g) as a solid, LC RT=5.66, δ (DMSO-d6) 7.65 (1H, s), 7.64 (1H, d, J 9.2 Hz), 7.47 (1H, m), 7.42 (1H, m), 7.31 (2H, s), 3.50 (2H, t, J 6.9 Hz), 3.34 (4H, m), 2.66 (2H, t, J 7.5 Hz), 1.78 (2H, m), 1.62 (2H, m), 1.49 (4H, m), 1.37 (2H, m), 1.30 (2H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07442719B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-e0b0b255cdd843f1b96bcce0880d6e1f
출처 메모uspto-grants-2008_10