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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 424177생성일: 2026년 10월 25일

Benzylamine → 2-Benzylamino-5-nitro-benzenesulfonamide

https://huagongshe.com/reaction/424177

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물TriethylamineHCID 8471—
반응물2-Chloro-5-nitrobenzenesulfonamideHCID 66784—
용매AcetonitrileHCID 6342—
생성물2-Benzylamino-5-nitro-benzenesulfonamideHCID 2485839784%

반응 조건

온도92 °C

반응 단계

A mixture of 2-chloro-5-nitro-benzenesulfonamide (2.20 kg, 9.30 mol), benzylamine (1.5 L, 13.9 mol), triethylamine (2.5 L, 18.1 mol), and acetonitrile (22.0 L) were heated at 92° C. for 20 h. The mixture was then cooled to 40° C., and was then partially concentrated in vacuo. The residue was added to 0° C. water (22.0 L) and the resulting suspension was allowed to warm to 23° C. and stirred for 2 h. The suspension was filtered and the solid was then washed with water (5 L). The washed solid was suspended in absolute ethanol (11 L), and was then filtered and washed with absolute ethanol (5 L). The solid was further dried in vacuo at 45° C. to afford the desired product, 2-benzylamino-5-nitro-benzenesulfonamide (2.40 kg, 7.81 mol, 84%), as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ: 4.64 (2H, d, J=4.6 Hz), 6.81 (1H, d, J=9.4 Hz), 7.23-7.44 (6H, m), 7.77 (2H, bs), 8.11 (1H, dd, J1=9.4 Hz, J2=2.3 Hz), 8.49 (1H, d, J=3.1 Hz). LC-MS (ESI) calcd for C13H13N3O4S 307.06, found 308.2 [M+H+] (100%), 615.2 [2M+H+] (81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101800B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-47e0fedc294b45d6963ded34a7f89be8
출처 메모uspto-grants-2012_01