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Dimethylformamide → 3-Phenylbenzo[b]thiophene-2-carbaldehyde

HRID 1906757
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HRID 1906757 반응식
C([Li])CCC.[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.CN(C)[CH:23]=[O:24]>O1CCCC1>[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][C:16]=2[CH:23]=[O:24])[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 6108813-PhenylbenzothiopheneHCID 178418339Butyllithium

생성물 1

HCID 105141003-Phenylbenzo[b]thiophene-2-carbaldehyde

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-70 °C

실험 절차

Butyllithium (62.5 ml of 1.6M solution in hexane, 0.1 mole) was added dropwise to a stirred solution of 3-phenylbenzo[b]thiophene (21.0 g, 0.1 mole) in tetrahydrofuran (150 ml) at -70° C. The solution was stirred at -70° C. for 30 minutes and dimethylformamide (10 ml, 0.13 mole) was added. The resulting mixture was stirred at -70° C. for 30 minutes and then allowed to warm to ambient temperature. After a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M) and the tetrahydrofuran removed under reduced pressure. The resulting oil was extracted into diethyl ether, the ethereal extract washed with water, dried over potassium carbonate and concentrated.

후처리

  1. stirringThe resulting mixture was stirred at -70° C. for 30 minutes
  2. temperatureto warm to ambient temperature
  3. customAfter a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M)
  4. customthe tetrahydrofuran removed under reduced pressure
  5. extractionThe resulting oil was extracted into diethyl ether
  6. extractionthe ethereal extract
  7. washwashed with water
  8. dry with materialdried over potassium carbonate
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6ab892673fc045028a5497921f9c43ee
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04654352

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