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醋酸 → Methyl 3-[(2-fluoroanilino)methyl]benzoate

HRID 1754315
笔记
打印预览

反应方程式

HRID 1754315 反应方程式
[CH:1]([C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7])=O.[F:13][C:14]1[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=1[NH2:16].C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl.O>[F:13][C:14]1[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=1[NH:16][CH2:1][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7]
参与物实验过程后处理来源与证据反应笔记

参与物

7

反应物 4

HCID 176醋酸HCID 9584邻氟苯胺HCID 6391453-甲醛苯甲酸甲酯HCID 5049666三乙酰氧基硼氢化钠

产物 1

HCID 86720274Methyl 3-[(2-fluoroanilino)methyl]benzoate收率 99.4%

试剂、催化剂与溶剂 2

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]溶剂
HCID 6344
二氯甲烷
溶剂
2 次

实验过程

To a stirred solution of methyl 3-formylbenzoate (1 g, 6.092 mmol) in anhydrous DCM (30 mL) was added 2-fluoroaniline (0.620 mL, 6.396 mmol) followed by glacial acetic acid (0.350 mL, 6.092 mmol). The reaction was stirred at room temperature for 18 hours. Sodium triacetoxyborohydride (3.23 g, 15.23 mmol) was added, and the reaction was stirred at room temperature for 3 hours. Water was added to quench the reaction, and the mixture was diluted with DCM. The organic layer was washed with brine, passed through a hydrophobic fit and the solvent was removed in vacuo to afford the title compound as a yellow oil (1.57 g, quantitative yield).

后处理

  1. stirringthe reaction was stirred at room temperature for 3 hours
  2. customto quench
  3. customthe reaction
  4. washThe organic layer was washed with brine
  5. customthe solvent was removed in vacuo

来源与证据

ORD记录
ord-f813ef39248c46d1a314020f7fc22839
来源数据集
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
专利号
US09169245B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记