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Ethyl bromoacetate → HCID 131727366、化合物

HRID 1785475
ノート
印刷プレビュー

反応式

HRID 1785475 の反応式
[CH2:1]([NH:8][NH:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1COCC1.Br[CH2:23][C:24]([O:26]CC)=[O:25]>CCCC[N+](CCCC)(CCCC)CCCC.[I-].CCN(CC)CC>[NH2:8][CH2:23][C:24]([OH:26])=[O:25].[CH2:1]([NH:8][NH:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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 7748Ethyl bromoacetate2 回HCID 8028TetrahydrofuranHCID 408153HCID 408153、化合物

生成物 1

HCID 131727366HCID 131727366、化合物収率 97%

試薬・触媒・溶媒 2

HCID 67553Tetrabutylammonium Iodide触媒HCID 8471Triethylamine溶媒2 回

反応条件

温度
60 °C

実験手順

To a solution of dibenzylhydrazine (5.30 g, 25.0 mmol) and THF (50 mL) and TBAI (0.46 g, 1.25 mmol) was added BrCH2CO2Et (2.64 mL, 23.8 mmol) and Et3N (3.32 mL, 23.8 mmol). The reaction mixture was stirred at 60° C. for 7 hours, an additional 0.3 eq. of base and electrophile were added (BrCH2CO2Et, 0.83 mL, 7.5 mmol and Et3N, 1.0 mL, 7.5 mmol). The reaction mixture was held overnight at R/T, an additional 0.3 eq. of each reagent was added and the reaction mixture was stirred at 60° C. for 4 more hours. The reaction mixture was partitioned with CH2Cl2, and the isolated organic fraction was washed with brine three (3 times), dried over Na2SO4, and concentrated in vacuo to afford 7.21 g, 24.2 mmol, (97%) of a crude oil.

後処理

  1. waitThe reaction mixture was held overnight at R/T
  2. stirringthe reaction mixture was stirred at 60° C. for 4 more hours
  3. customThe reaction mixture was partitioned with CH2Cl2
  4. washthe isolated organic fraction was washed with brine three (3 times)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ebeeb039964a4f5b90012c8ce5c1b9a9
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07504521B2

反応ノート

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