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

HRID 1186896
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HRID 1186896 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

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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 1M 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-7545fb8832b6405c8f546a1283b19197
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08673924B2

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