Hydrochloric Acid → Ethyl 1-(4-bromophenyl)cyclopentane-1-carboxylate

HRID 2391064ノート

反応式

HRID 2391064 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:4][CH:3]=1.[H-].[Na+].Br[CH2:17][CH2:18][CH2:19][CH2:20]Br.Cl>CN(C=O)C.CCOC(C)=O>[CH2:12]([O:11][C:9]([C:8]1([C:5]2[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=2)[CH2:20][CH2:19][CH2:18][CH2:17]1)=[O:10])[CH3:13]

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 80561,4-DibromobutaneHCID 24758Sodium hydrideHCID 7020609Ethyl 2-(4-bromophenyl)acetate

生成物 1

HCID 66660571Ethyl 1-(4-bromophenyl)cyclopentane-1-carboxylate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of ethyl 4-bromophenylacetate (2 g, 8.2 mmol) in DMF (20 mL) at 0° C. was added sodium hydride (60% in mineral oil; 0.72 g, 18.1 mmol), and the mixture was stirred for 10 minutes. 1,4-Dibromobutane (1.07 mL, 9.0 mmol) was added, and the reaction was stirred at room temperature for 30 minutes. Once no starting material was seen by analytical tlc, the mixture was worked up with EtOAc and aqueous 10% HCl, and the crude material was purified by silica gel chromatography to give the title compound.

後処理

  1. stirringthe reaction was stirred at room temperature for 30 minutes
  2. customthe crude material was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-8604a3d5190d4b1ca22e518064c25665
出典データセット
uspto-grants-2012_09
特許番号
US08273780B2

反応ノート

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