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HRID 81549作成日:2026年10月23日
Benzene, 1-bromo-3-iodo- → 2-(3-Bromo-phenyl)-2-tert-butoxycarbonylamino-3,3,3-trifluoro-propionic acid ethyl ester
https://huagongshe.com/ja/reaction/81549
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Benzene, 1-bromo-3-iodo- | HCID 11561 | — |
| 反応物 | Ethyl 2-((tert-butoxycarbonyl)imino)-3,3,3-trifluoropropanoate | HCID 5706451 | — |
| 反応物 | HCID 178418918 | HCID 178418918 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(3-Bromo-phenyl)-2-tert-butoxycarbonylamino-3,3,3-trifluoro-propionic acid ethyl ester | HCID 66665703 | — |
反応手順
A solution of 5.66 g (20 mmol) 1-bromo-3-iodo-benzene in 25 ml THF was stirred at −20° C. A 1.82 M solution of isopropylmagnesium chloride (12.1 ml, 22.0 mmol) in THF was added and the mixture was stirred 1 h at 0° C. The mixture was cooled to −78° C. and a solution of 5.38 g (20 mmol) 2-[(E)-tert-butoxycarbonylimino]-3,3,3-trifluoro-propionic acid ethyl ester in 50 ml of THF was added over a period of 2 h. After 20 min the mixture was quenched with 5% aqueous NH4Cl. The mixture was extracted with TBME. The organic phase was dried with Na2SO4, filtered and evaporated. Purification via chromatography on silica gel (c-hexane/0-14% EtOAc) gave the desired product as a colorless resin.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846658B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-0fe51288042c4bebbc75f7123b607156 |
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| 出典メモ | uspto-grants-2014_09 |
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