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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1468161생성일: 2026년 10월 26일

Acetic Acid → 3-[4-(3-Cyano-phenyl)-piperazin-1-ylmethyl]-benzoic acid methyl ester

https://huagongshe.com/reaction/1468161

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물Methyl 3-formylbenzoateHCID 639145—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(3-Cyanophenyl)piperazineHCID 11480902—
용매1,1-DichloroethaneHCID 6365—
생성물3-[4-(3-Cyano-phenyl)-piperazin-1-ylmethyl]-benzoic acid methyl esterHCID 6750819080.5%

반응 단계

Dissolve 3-piperazin-1-yl-benzonitrile (0.19 g, 1.00 mmol), 3-formyl-benzoic acid methyl ester (0.33 g, 2.00 mmol) and AcOH (0.64 mL, 10.0 mmol) in 5 mL dichloroethane. Add NaBH(OAc)3 (0.42 g, 2.00 mmol) and stir the mixture overnight. Add another portion of NaBH(OAc)3 (0.42 g, 2.00 mmol) and stir the mixture an additional 24 h. Concentrate the crude reaction mixture under a stream of N2. Dissolve the residue into 5% HCl and apply to a Dowex column. Wash the column with 1×50 mL 5% HCl, 2×50 mL H2O, 2×50 mL of MeOH and 2×50 mL of dichloromethane. Liberate the basic residues by washing the resin with 3×30 mL of 10% NH3/MeOH and 2×20 mL of dichloromethane. Concentrate the basic washings to give 0.27 g of 3-[4-(3-cyano-phenyl)-piperazin-1-ylmethyl]-benzoic acid methyl ester as a clear oil. 1H NMR indicates some contamination with starting amine. The mixture is carried on without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09000154B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-8d4599e273644e549f60421d34e908be
출처 메모uspto-grants-2015_04