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HRID 1417809생성일: 2026년 10월 26일

1-Formyl-4-(2-bromo-4-methoxyphenyl)piperazine → 1-(2-Bromo-4-methoxyphenyl)piperazine

https://huagongshe.com/reaction/1417809

반응식

참여 물질

역할이름HCID투입량
반응물1-Formyl-4-(2-bromo-4-methoxyphenyl)piperazineHCID 23288818—
용매Hydrochloric AcidHCID 313—
생성물1-(2-Bromo-4-methoxyphenyl)piperazineHCID 23288928—

반응 단계

A mixture of 1-formyl-4-(2-bromo-4-methoxyphenyl)piperazine (VII, 3.92 g, 3.1 mmol) and hydrochloric acid (4N, 70 ml) is heated at 100° for 50 min. The mixture is then concentrated under reduced pressure to remove most of the aqueous hydrochloric acid. Saturated sodium bicarbonate is then cautiously added and the aqueous phase is extracted with dichloromethane. The combined organic phase is backwashed with saline, dried over magnesium sulfate, and concentrated to give 1-(2-bromo-4-methoxyphenyl)piperazine (VIII), NMR (CDCl3) 2.55, 2.95, 3.08, 3.77, 6.83, 7.01, 7.14 δ.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05877317
출처 데이터셋uspto-grants-1999_03
ORD IDord-adba3b0f6a4f4aa382e2cf38ed387201
출처 메모uspto-grants-1999_03