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Ammonium Chloride → 1-(4-(Trifluoromethoxy)phenyl)propan-1-ol

HRID 594311
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HRID 594311 반응식
[F:1][C:2]([F:13])([F:12])[O:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[O:9])=[CH:6][CH:5]=1.[CH2:14]([Mg]Br)[CH3:15].[NH4+].[Cl-]>C1COCC1>[F:1][C:2]([F:12])([F:13])[O:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]([OH:9])[CH2:14][CH3:15])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 69573p-(Trifluoromethoxy)benzaldehydeHCID 178418443HCID 178418443, 화합물

생성물 1

HCID 534664281-(4-(Trifluoromethoxy)phenyl)propan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A cooled (0° C.) solution of 4-(trifluoromethoxy)benzaldehyde (5.000 g; 26.29 mmol) in anh. THF (50 ml) was treated dropwise with a solution of ethylmagnesium bromide (3 M in Et2O; 10.50 ml; 31.50 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 17 h. The resulting reaction mixture was cooled to 0° C., and aq. sat. NH4Cl (30 ml) was added dropwise. The separated aq. layer was further extracted with AcOEt (3×20 ml), and the mixed organic layers were dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=60/1) afforded 1-(4-(trifluoromethoxy)phenyl)propan-1-ol as a colorless oil. LC-MS (conditions A): tR=0.79 min.; no ionisation.

후처리

  1. customThe resulting reaction mixture
  2. temperaturewas cooled to 0° C.
  3. extractionThe separated aq. layer was further extracted with AcOEt (3×20 ml)
  4. dry with materialthe mixed organic layers were dried over anh. MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated to dryness under reduced pressure
  7. customPurification by FC (DCM/MeOH=60/1)

출처 및 근거

ORD 기록
ord-08ad95d6ed974d70b34f0764a6a21dae
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242970B2

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