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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127473생성일: 2026년 10월 26일

Hydrochloric Acid → Methyl 2-hydroxy-5-[2-[4-(2-methylphenyl)-1-piperazinyl]acetyl]benzoate dihydrochloride

https://huagongshe.com/reaction/127473

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물2-MeppHCID 91965—
반응물Triethylammonium bromideHCID 2734074—
반응물Methyl 5-(2-bromoacetyl)-2-hydroxybenzoateHCID 11601501—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-hydroxy-5-[2-[4-(2-methylphenyl)-1-piperazinyl]acetyl]benzoate dihydrochlorideHCID 20287077—

반응 단계

A solution of 10.9 g (0.04 mol) of methyl 5-(2-bromoacetyl)-2-hydroxybenzoate in 100 ml of dry tetrahydrofuran is added dropwise over 4 hours to a stirred solution of 7.1 g (0.04 mol) of 1-(2-methylphenyl)piperazine and 4.0 g (0.04 mol) of triethylamine in 75 ml of tetrahydrofuran at room temperature. Stirring is continued for 2-12 hours or until the theoretical amount (7.3 g) of triethylamine hydrobromide precipitates. The precipitates is removed by filtration and the filtrate is evaporated to dryness. Addition of 2 equivalents of methanolic HCl and precipitation by addition of ethyl ether at room temperature affords the crude methyl 2-hydroxy-5-[2-[4-(2-methylphenyl)-1-piperazinyl]acetyl]benzoate dihydrochloride (9.4 g). Attempts to purify this product by recrystallization frequently led to decomposition and were subsequently avoided.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255575
출처 데이터셋uspto-grants-1981_03
ORD IDord-35f46730076441c895e1fb9d05cddd04
출처 메모uspto-grants-1981_03