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Borane;tetrahydrofuran → 4-(5-Oxazolyl)benzylamine

HRID 1243870
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HRID 1243870 반응식
[O:1]1[C:5]([C:6]2[CH:14]=[CH:13][C:9]([C:10]([NH2:12])=O)=[CH:8][CH:7]=2)=[CH:4][N:3]=[CH:2]1.B.C1COCC1>C1COCC1>[O:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]([CH2:10][NH2:12])=[CH:13][CH:14]=2)=[CH:4][N:3]=[CH:2]1
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참가 물질

4

반응물 2

HCID 2723981Borane;tetrahydrofuranHCID 219309994-(5-Oxazolyl)-benzamide

생성물 1

HCID 219309934-(5-Oxazolyl)benzylamine수율 32.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
0 °C

실험 절차

A suspension of 4-(5-oxazolyl)benzamide (500 mg, 2.657 mmol) in 10 mL of dry THF was cooled to 0° C. and 10 mL of 1 M BH3.THF (10.00 mmol) was added. The contents were refluxed overnight and the excess borane was destroyed by dropwise addition of methanol. The solvent was evaporated and the residue was treated with methanolic HCl to decompose the amine-borane complex. After evaporation of the methanol, the residue was taken in water, basified to pH 10 and the product was extracted in to DCM. The DCM layer was dried (K2CO3) and the solvent was removed to provide 150 mg (32%) of 4-(5-oxazolyl)benzylamine: 1H NMR (CDCl3) δ 7.90 (s, 1H), 7.60 (d, 2H), 7.40 (d, 2H), 7.30 (s, 1H), 3.90 (s, 2H).

후처리

  1. temperatureThe contents were refluxed overnight
  2. customthe excess borane was destroyed by dropwise addition of methanol
  3. customThe solvent was evaporated
  4. additionthe residue was treated with methanolic HCl
  5. customAfter evaporation of the methanol
  6. extractionthe product was extracted in to DCM
  7. dry with materialThe DCM layer was dried (K2CO3)
  8. customthe solvent was removed

출처 및 근거

ORD 기록
ord-ec97c137ad914143a00d2238022a416b
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07119200B2

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