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Triphenylphosphine → 2-Propenal, 3-(1-naphthalenyl)-, (E)-

HRID 1743957
ノート
印刷プレビュー

反応式

HRID 1743957 の反応式
[C:1]1([CH:11]=[CH:12][C:13](Cl)=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>CC(C)=O>[C:1]1([CH:11]=[CH:12][CH:13]=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 11776TriphenylphosphineHCID 534112803-(Naphthalen-1-yl)prop-2-enoyl chloride

生成物 1

HCID 6024602-Propenal, 3-(1-naphthalenyl)-, (E)-収率 79%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a stirred solution of 3-(1-naphthalenyl)-2-propenoyl chloride (2.5 g, 0.012 mol) and 6.03 g (0.023 mol) of triphenyl phosphine in 50 ml of acetone was added 7.65 g (0.013 mol) of bis(triphenylphosphine)tetrahydroboratocopper in one portion. After an hour the solution was filtered and the filtrate was evaporated to dryness. The residue was dissolved in 20 ml of chloroform and treated with 6 g of cuprous chloride, allowed to stir for an hour and filtered. The solvent was evaporated to dryness to yield 1.66 g (79 percent) of solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationAfter an hour the solution was filtered
  2. customthe filtrate was evaporated to dryness
  3. dissolutionThe residue was dissolved in 20 ml of chloroform
  4. additiontreated with 6 g of cuprous chloride
  5. filtrationfiltered
  6. customThe solvent was evaporated to dryness

出典と根拠

ORDレコード
ord-93263f872ff54764a27a5ccb03a20505
出典データセット
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07012121B2

反応ノート

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