참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | 2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine | HCID 21942269 | — |
| 반응물 | HCID 178419663 | HCID 178419663 | — |
| 촉매 | Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chloride | HCID 21654969 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine | HCID 21942262 | — |
반응 단계
A mixture of 6.3 g of 2-bromo-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine, 240 mg of 1,3-bis(diphenylphosphino)propanenickel (II) chloride and 20 ml of tetrahydrofuran was stirred in advance under nitrogen atmosphere in an ice bath. To this was added dropwise a diethyl ether solution of benzyl magnesium bromide prepared from 3.4 ml of benzyl bromide, 0.8 g of magnesium and 15 ml of diethyl ether, followed by stirring as it was at room temperature for overnight. The reaction mixture was partitioned between a saturated aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography with 5–10% ethyl acetate/hexane, to give 6.6 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07112593B2 |
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| 출처 데이터셋 | uspto-grants-2006_09 |
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| ORD ID | ord-7efc740474614fa8bb53d2db1bac1da8 |
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| 출처 메모 | uspto-grants-2006_09 |
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