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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1706100생성일: 2026년 10월 26일

4-(Chloromethyl)-2-nitroanisole → Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1)

https://huagongshe.com/reaction/1706100

반응식

참여 물질

역할이름HCID투입량
반응물4-(Chloromethyl)-2-nitroanisoleHCID 80785—
반응물Formamide, N,N'-[(methylimino)di-3,1-propanediyl]bis-HCID 3084810—
용매AcetonitrileHCID 6342—
생성물Benzenemethanaminium, N,N-bis[3-(formylamino)propyl]-4-methoxy-N-methyl-3-nitro-, chloride (1:1)HCID 100848—

반응 단계

A mixture of 54.0 parts of N,N-bis(3-formamidopropyl)methylamine, 50.4 parts of 4-methoxy-3-nitrobenzyl chloride, and 78 parts of acetonitrile was stirred at reflux for seven and a half hours. An additional 78 parts of acetonitrile was added to the reaction mixture causing an oil to separate. Heating at reflux was continued for an additional two hours and the 140 parts of acetonitrile was distilled away and 200 parts of water was added. The remaining acetonitrile was removed by distillation and the cooled reaction mixture was filtered with the aid of diatomaceous earth to obtain an aqueous solution of N-methyl-N-(3-nitro-4-methoxybenzyl)-N,N-bis(3-formamidopropyl)ammonium chloride. The solution was used directly for reduction of the nitro group.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04206144
출처 데이터셋uspto-grants-1980_06
ORD IDord-bd78798aed8c4192a6fd2401ef552fec
출처 메모uspto-grants-1980_06