関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | methyl 3-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]benzoate | HCID 90072367 | — |
| 反応物 | HCID 178443585 | HCID 178443585 | — |
| 反応物 | HCID 178467792 | HCID 178467792 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate | HCID 86713465 | — |
反応手順
To a solution of 500 mg of methyl 3-[(E)-{[(S)-tert-butylsulfinyl]imino}methyl]benzoate in 12 ml of THF was added 0.50 ml of a 1 M diethylzinc/hexane solution at −78° C., followed by stirring at the same temperature for 5 minutes. 0.80 ml of a 3 M ethylmagnesium bromide/diethyl ether solution was added thereto at −78° C., followed by stirring at the same temperature for 2 hours. To the reaction mixture were added a saturated aqueous ammonium chloride solution and ethyl acetate to carry out a layer separation operation. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 447 mg of methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09447090B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-bfc183d973b3464fa90f16ef138d3c7f |
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| 出典メモ | uspto-grants-2016_09 |
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