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Triethylamine → 2-Methyl-2-(2-nitro-phenylamino)-propionic acid tert-butyl ester

HRID 1747408
ノート
印刷プレビュー

反応式

HRID 1747408 の反応式
F[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].Cl.[C:12]([O:16][C:17](=[O:22])[C:18]([NH2:21])([CH3:20])[CH3:19])([CH3:15])([CH3:14])[CH3:13].CCN(CC)CC>CN(C=O)C.CCOC(C)=O>[C:12]([O:16][C:17](=[O:22])[C:18]([CH3:20])([NH:21][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9])[CH3:19])([CH3:15])([CH3:13])[CH3:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8471TriethylamineHCID 738951-Fluoro-2-nitrobenzeneHCID 12186776Tert-butyl 2-amino-2-methylpropanoate hydrochloride

生成物 1

HCID 594976512-Methyl-2-(2-nitro-phenylamino)-propionic acid tert-butyl ester収率 50%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒
HCID 8857
Ethyl Acetate
溶媒

反応条件

温度
85 °C

実験手順

To a mixture of 1-fluoro-2-nitrobenzene (485 μL, 4.6 mmol) and 2-amino-2-methyl-propionic acid tert-butyl ester hydrochloride (1.0 g, 5.1 mmol) in DMF (5 mL) was added Et3N (1.3 mL, 9.3 mmol). The mixture was heated at 85° C. for 16 hours. The reaction mixture was allowed to cool to room temperature, diluted with EtOAc (50 mL) and washed with H2O (50 mL×3). The organic layer was dried over sodium sulfate and concentrated. The resulting residue was purified by CombiFlash with 10% EtOAc in Hexane as the eluent to afford the desired 2-methyl-2-(2-nitro-phenylamino)-propionic acid tert-butyl ester (640 mg, 50%).

後処理

  1. temperatureto cool to room temperature
  2. washwashed with H2O (50 mL×3)
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. concentrationconcentrated
  5. customThe resulting residue was purified by CombiFlash with 10% EtOAc in Hexane as the eluent

出典と根拠

ORDレコード
ord-a56a2960a3f54036a5b1cb5607203a81
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150556B2

反応ノート

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