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

HRID 1743957
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반응식

HRID 1743957 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-93263f872ff54764a27a5ccb03a20505
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07012121B2

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