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1,2-Dibromoethane → Ethyl 4-(3,4-dichlorobenzyl)benzoate

HRID 2359339
ノート
印刷プレビュー

反応式

HRID 2359339 の反応式
[Cl-].[Li+].BrCCBr.Br[CH2:8][C:9]1[CH:19]=[CH:18][C:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:11][CH:10]=1.[Cl:20][C:21]1[CH:22]=[C:23](I)[CH:24]=[CH:25][C:26]=1[Cl:27].[Cl-].[NH4+]>C1COCC1.[Zn].CC(C1C=CC=C(C(C)C)C=1N1[CH-]N(C2C(C(C)C)=CC=CC=2C(C)C)CC1)C.C1C=NC=C(Cl)C=1.Cl[Pd]Cl.C[Si](Cl)(C)C>[Cl:20][C:21]1[CH:22]=[C:23]([CH:24]=[CH:25][C:26]=1[Cl:27])[CH2:8][C:9]1[CH:19]=[CH:18][C:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 5

HCID 78391,2-DibromoethaneHCID 25517Ammonium ChlorideHCID 88591Benzene, 1,2-dichloro-4-iodo-HCID 433294Lithium ChlorideHCID 954261Ethyl 4-(bromomethyl)benzoate

生成物 1

HCID 58046347Ethyl 4-(3,4-dichlorobenzyl)benzoate収率 53.9%

試薬・触媒・溶媒 4

HCID 6397Chlorotrimethylsilane触媒
HCID 23994Zinc触媒2 回
HCID 588388791,3-Bis[2,6-di(propan-2-yl)phenyl]imidazolidin-2-ide;3-chloropyridine;dichloropalladium触媒
HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A mixture of zinc (404 mg, 6.17 mmol) and lithium chloride (261 mg, 6.17 mmol) under argon was warmed for 15 minutes using a hot air gun, allowed to cool and then anhydrous THF (20 mL) added. The zinc was activated by treatment with 1,2-dibromoethane (19 mg, 0.10 mmol) and TMSCl (2.2 mg, 0.02 mmol). To the resulting mixture at 25° C. was added ethyl 4-(bromomethyl)benzoate (500 mg, 2.06 mmol) and the mixture stirred for 15 minutes. A solution of 3,4-dichloro-iodobenzene (392 mg, 1.44 mmol) in anhydrous THF (5 mL) was added, followed by (1,3-bis(2,6-diisopropylphenyl)imidazolidene)(3-chloropyridyl)palladium(II) dichloride [PEPPSI™-SlP] (14 mg, 0.02 mmol) and the mixture stirred at 25° C. for 1 hour. Saturated ammonium chloride solution was added and the crude product extracted with ether. The ether extract was washed with brine, dried over Na2SO4 and the solvent evaporated in vacuo. The crude product was purified by silica gel column chromatography eluting with 7:3 hexane:ethyl acetate to afford the title compound (240 mg, 38%).

後処理

  1. temperaturewas warmed for 15 minutes
  2. temperatureto cool
  3. stirringthe mixture stirred at 25° C. for 1 hour
  4. extractionthe crude product extracted with ether
  5. extractionThe ether extract
  6. washwas washed with brine
  7. dry with materialdried over Na2SO4
  8. customthe solvent evaporated in vacuo
  9. customThe crude product was purified by silica gel column chromatography
  10. washeluting with 7:3 hexane

出典と根拠

ORDレコード
ord-a67f175506ca4c13b9a89e3bc33e3cca
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08685977B2

反応ノート

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