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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 342624생성일: 2026년 10월 27일

Citric Acid → 3-(4-Cyanobenzyl)pyridin-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/342624

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Ethyl AcetateHCID 8857—
반응물4-(Bromomethyl)benzonitrileHCID 86996—
반응물Methyl 3-bromoisonicotinateHCID 2762700—
촉매ZincHCID 23994—
촉매HCID 178418751HCID 178418751—
용매TetrahydrofuranHCID 8028—
생성물3-(4-Cyanobenzyl)pyridin-4-carboxylic acid methyl esterHCID 53953426—

반응 단계

A solution of 4-cyanobenzyl bromide (625 mg, 3.27 mmol) in dry THF (4 mL) was added slowly over ~3 min. to a suspension of activated Zn (dust; 250 mg) in dry THF (2 mL) at 0° under an argon atmosphere. The ice-bath was removed and the slurry was stirred at room temperature for a further 30 min. Then 3-bromopyridin-4-carboxylic acid methyl ester (540 mg. 2.5 mmol) followed by dichlorobis(triphenylphosphine)nickel (II) (50 mg). The resultant reddish-brown mixture was stirred for 3 h at ~40°-45° C. The mixture was cooled and distributed between EtOAc (100 ml,) and 5% aqueous citric acid (50 mL). The organic layer was washed with H2O(2×50 mL), dried with Na2SO4. After evaporation of the solvent the residue was purified on silica gel, eluting with 35% EtOAc in hexane to give 420 mg as a clear gum. FAB ms (M+1)253.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05859012
출처 데이터셋uspto-grants-1999_01
ORD IDord-b2cf0ecfa5e14d46bc4ce3065a213a40
출처 메모uspto-grants-1999_01