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Diisobutylaluminumhydride → 2-(Trifluoromethyl)pyrimidine-5-carbaldehyde

HRID 1047609
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HRID 1047609 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[N:8]=[CH:7][C:6]([C:9](OCC)=[O:10])=[CH:5][N:4]=1.[H-].C([Al+]CC(C)C)C(C)C>ClCCl>[F:15][C:2]([F:1])([F:14])[C:3]1[N:4]=[CH:5][C:6]([CH:9]=[O:10])=[CH:7][N:8]=1
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참가 물질

4

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 21936133Ethyl 2-(trifluoromethyl)pyrimidine-5-carboxylate

생성물 1

HCID 177509412-(Trifluoromethyl)pyrimidine-5-carbaldehyde수율 138.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

To a solution of ethyl 2-(trifluoromethyl)pyrimidine-5-carboxylate (25.5 g, 116.0 mmol) in dichloromethane (580 mL) at −78° C. was slowly added diisobutylaluminium hydride (1.0 M; 130.0 mL, 130.0 mmol). The mixture was stirred at −78° C. After 2 h, the mixture was quenched via slow addition of hydrochloric acid (2.0 M). The mixture was allowed to warm to ambient temperature. The mixture was extracted with diethyl ether (3×). The combined organic extracts was dried over sodium sulfate, filtered and concentrated to give the title compound (28.2 g).

후처리

  1. customat −78° C.
  2. customthe mixture was quenched via slow addition of hydrochloric acid (2.0 M)
  3. temperatureto warm to ambient temperature
  4. extractionThe mixture was extracted with diethyl ether (3×)
  5. dry with materialThe combined organic extracts was dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2032114121ad44bdb8426a84ed31d0ff
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08569512B2

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