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HRID 74779作成日:2026年10月24日
N-(9-Fluorenylmethoxycarbonyloxy)succinimide → 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoic acid
https://huagongshe.com/ja/reaction/74779
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-(9-Fluorenylmethoxycarbonyloxy)succinimide | HCID 134122 | — |
| 反応物 | 3-Amino-2,2-dimethylpropanoic acid hydrochloride | HCID 53407724 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 溶媒 | Sodium Carbonate | HCID 10340 | — |
| 生成物 | 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoic acid | HCID 45024431 | 99.7% |
反応手順
A solution of 3-amino-2,2-dimethylpropanoic acid hydrochloride (1.0 g, 6.5 mmol, 1.0 eq.) in 10 mL of 10% Na2CO3 was added to a solution of 1-{[(9H-fluoren-9-ylmethoxy)carbonyl]oxy}pyrrolidine-2,5-dione (2.3 g, 6.5 mmol, 1.0 eq.) in 10 mL of DME. The reaction was allowed to stir at room temperature overnight. Reaction was concentrated to a smaller volume and then washed two times with ether. The aqueous layer was acidified to pH<2 with concentrated HCl and then extracted three times with a 10% methanol 90% dichloromethane solution. The organics where combined before being washed with 1M HCl and brine. The organic layer was dried over sodium sulfate and concentrated in vacuo producing #124 (2.2 g, 98%) as a white solid. LC-MS (Protocol Q1): m/z 362.0 [M+Na+] retention time=0.89 minutes.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08828401B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-278e8d3542b44196a5b3f59e1bada9f9 |
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| 出典メモ | uspto-grants-2014_09 |
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