関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| 反応物 | Ethyl Cinnamate | HCID 637758 | — |
| 反応物 | dimethylsulfoxide THF | HCID 21830753 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | Ethyl trans-2-phenylcyclopropanecarboxylate | HCID 252496 | 79% |
反応手順
To a stirred mixture of NaH (40.7 g) in DMSO (2.5 L) under N2 was added portion wise trimethyl sulfoxonium iodide (396 g, 1.80 mol, 1.76 equiv). A solution of 31 (180 g, 1.02 mol, 1.00 equiv) in 1:1 DMSO/THF (2 L) was added, and the reaction mixture was stirred at 25° C. overnight. The reaction mixture was quenched with 1N HCl (1 L) and extracted with EtOAc (2×2 L). The combined organic layers were washed with water (2×2 L) and brine (1×2 L), dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by SiO2 chromatography eluting with EtOAc/petroleum ether (5 to 12.5% EtOAc) to afford 153 g (79%) of trans-ethyl-2-phenylcyclopropane-1-carboxylate (33) as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08637537B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-7c5defb9202a4a73920355d3fd2b1232 |
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| 出典メモ | uspto-grants-2014_01 |
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