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2-Cyclopenten-1-one → Ethyl 2-oxobicyclo[3.1.0]hexane-6-carboxylate

HRID 1289907
ノート
印刷プレビュー

反応式

HRID 1289907 の反応式
[Br-].[C:2]([CH2:7][S+](C)C)([O:4][CH2:5][CH3:6])=[O:3].N12CCCN=C1CCCCC2.[C:22]1(=[O:27])[CH2:26][CH2:25][CH:24]=[CH:23]1.Cl.[Cl-].[Na+]>C1(C)C=CC=CC=1>[O:27]=[C:22]1[CH2:26][CH2:25][CH:24]2[CH:23]1[CH:7]2[C:2]([O:4][CH2:5][CH3:6])=[O:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 135882-Cyclopenten-1-oneHCID 78861(2-Ethoxy-2-oxoethyl)dimethylsulphonium bromideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 19796930Hydrochloridesodium chloride

生成物 1

HCID 565357Ethyl 2-oxobicyclo[3.1.0]hexane-6-carboxylate収率 68.3%

試薬・触媒・溶媒 1

HCID 1140
Toluene
溶媒

実験手順

A suspension of carboethoxymethyl dimethylsulfonium bromide (45.5 g) in toluene (350 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (30.2 g). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with 2-cyclopenten-1-one (19.57 g). After an additional 18 hours, the reaction mixture was added to a 1N hydrochloric acid/sodium chloride solution. The resulting mixture was extracted with diethyl ether. The combined ether extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified using silica-gel chromatography, eluting with a linear gradient of 10% ethyl acetate/hexanes to 50% ethyl acetate/hexanes, to give 22.81 g of the title compound. Melting point: 36°-38° C.

後処理

  1. waitAfter an additional 18 hours
  2. extractionThe resulting mixture was extracted with diethyl ether
  3. dry with materialThe combined ether extracts were dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified
  7. washeluting with a linear gradient of 10% ethyl acetate/hexanes to 50% ethyl acetate/hexanes

出典と根拠

ORDレコード
ord-09c753669ac0443e8dc995dcacdabdd5
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05750566

反応ノート

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