참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Citric Acid | HCID 311 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| 반응물 | Methyl 3-bromoisonicotinate | HCID 2762700 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 촉매 | HCID 178418751 | HCID 178418751 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(4-Cyanobenzyl)pyridin-4-carboxylic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05859012 |
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| 출처 데이터셋 | uspto-grants-1999_01 |
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| ORD ID | ord-b2cf0ecfa5e14d46bc4ce3065a213a40 |
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| 출처 메모 | uspto-grants-1999_01 |
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