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HRID 466364생성일: 2026년 10월 26일

Acetic Acid → N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromide

https://huagongshe.com/reaction/466364

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl BromideHCID 6332—
반응물N-(4-Acetyl-2-methylphenyl)methanesulfonamideHCID 19873430—
반응물N-[4-[2-(ethylheptylamino)ethyl]phenyl]methanesulfonamideHCID 53740092—
용매AcetonitrileHCID 6342—
생성물N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromideHCID 19873396—

반응 단계

A stirred solution of N-[4-[2-(ethylheptylamino)ethyl]phenyl]methanesulfonamide as prepared in Example 3 (0.332 g, 0.975 mmol) in acetonitrile (3 ml) is treated with HOAc, (0.056 ml, 0.975 mmol) and ethyl bromide (0.73 ml, 9.75 mmol). The solution is refluxed for 1 day, treated with additional ethyl bromide (1 ml) and acetonitrile (3 ml) and refluxed for one additional day. The mixture is concentrated; the residue is mixed with a solution of NaHCO3 (160 mg) in water and extracted with Et2O. The extracts are washed with water, dried (MgSO4) and concentrated to give recovered starting material (0.15 g, identified by TLC). The aqueous layers are combined, made strongly basic with 1N KOH, saturated with potassium bromide and washed with CH2Cl2. The aqueous layer is then acidified with 48% hydrogen bromide and extracted with CH2Cl2. The extracts are washed with saturated potassium bromide, dried (NaSO4) and concentrated to give 0.15 g of N,N-diethyl-N-heptyl-4-[(methylsulfonyl)amino]benzeneethanaminium bromide. MS calc'd for C20H37N2O2S (M+): 369.2576. Found: 369.2585.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155268
출처 데이터셋uspto-grants-1992_10
ORD IDord-e6e6ab513b7f4085a6d7b165e9cd6194
출처 메모uspto-grants-1992_10