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HRID 1250898생성일: 2026년 10월 26일

Ethylamine → N'-(6-Chloro-2-methyl-phenyl)-N-ethyl-propane-1,3-diamine

https://huagongshe.com/reaction/1250898

반응식

참여 물질

역할이름HCID투입량
반응물EthylamineHCID 6341—
반응물1-(6-Chloro-2-methyl-phenyl)amino-3-hydroxy-propaneHCID 18324834—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N'-(6-Chloro-2-methyl-phenyl)-N-ethyl-propane-1,3-diamineHCID 1832482254.3%

반응 단계

A mixture of a 2.0 M solution of ethylamine in tetrahydrofuran (139.5 mL) and the hydrobromide salt of Example 12, Step A (9.5 g) was stirred at ambient temperature under nitrogen for 48 hours. The tetrahydrofuran was removed in vacuo and the residue was partitioned between dichloromethane and 1N sodium hydroxide. The extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo to give a brown oil. The crude material was dissolved in dichloromethane and absorbed onto a column of Merck-60 flash silica gel. Elution with a solvent gradient (from 95:5 to 80:20 dichloromethane-methanol containing 0.2% ammonium hydroxide) gave the title compound (3.4 g, 54.3%) as a yellow oil, which was used as such in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06340687B1
출처 데이터셋uspto-grants-2002_01
ORD IDord-87b31028294e4602931608be0f5cbc66
출처 메모uspto-grants-2002_01