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HRID 855238생성일: 2026년 10월 25일

Water → N'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamine

https://huagongshe.com/reaction/855238

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-tert-ButylbenzaldehydeHCID 70324—
반응물1,2-Ethanediamine, N1-ethyl-N1-(3-methylphenyl)-HCID 87984—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물N'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamineHCID 6934286595%

반응 단계

1.62 g (10 mmol) of 4-tert-butyl benzaldehyde and 1.78 g (10 mmol) of N*1*-ethyl-N*1* -m-tolyl-ethane-1,2-diamine were dissolved in 20 ml methanol and the solution was stirred for 2 h at rt. 567 mg (15 mmol) of sodium borohydride were added in portions under nitrogen. The reaction mixture was stirred at rt over night. Water was added and the solvent was evaporated. The reaction mixture was extracted with diethyl ether and the organic layer was washed with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated to leave the 3.08 g (95%) product as a light yellow oil. 1H NMR (DMSO-d6, 300 MHz): δ 7.33 (d, 2H), 7.24 (d, 2H), 7.09 (dd, 1H), 6.51 (m, 3H), 3.78 (s, 2H), 3.42 (t, 2H), 3.34 (q, 2H), 2.85 (t, 2H), 2.29 (s, 3H), 1.31 (s, 9H), 1.11 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07259183B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-f8163ec0f6c446e3a9d9efb6fbe68099
출처 메모uspto-grants-2007_08