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1-Phenylcyclopropanecarboxamide → 1-Phenylcyclopropanemethanamine

HRID 1685317
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HRID 1685317 반응식
[C:1]1([C:7]2([C:10]([NH2:12])=O)[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>O1CCCC1>[C:1]1([C:7]2([CH2:10][NH2:12])[CH2:8][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 2922171-PhenylcyclopropanecarboxamideHCID 21226445Aluminium lithium hydride

생성물 1

HCID 702871-Phenylcyclopropanemethanamine수율 49%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
65 °C

실험 절차

A solution of 1-phenylcyclopropanecarboxamide (0.450 g, 2.79 mmol) in tetrahydrofuran (5 mL) was slowly added to a suspension of LAH (0.117 g, 3.07 mmol) in tetrahydrofuran (5 mL) at 23° C. over 2 minutes. The reaction was then heated to 65° C. for 6 hours. The reaction was quenched with the Rochelle salt (1N in water, 10 mL) and extracted with ethyl acetate (3×). The combined organic layers were then dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude title material (0.200 g, 49%) as an oil which was used as such in the next reaction. An aliquot was purified on preparative HPLC (ammonium acetate/water/acetonitrile). 1H NMR (400 MHz, CDCl3, acetic acid salt) δ: 0.83-0.94 (4H, m), 1.98 (3H, s), 2.90 (2H, s), 4.98 (3H, br s), 7.23-7.37 (5H, m).

후처리

  1. customThe reaction was quenched with the Rochelle salt (1N in water, 10 mL)
  2. extractionextracted with ethyl acetate (3×)
  3. dry with materialThe combined organic layers were then dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-fab299aae0f546779a72abe5a7e82cf8
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148400B2

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