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N-(2-hydroxy-2-phenylethyl)pent-4-ynamide → Pent-4-ynoic acid (2-oxo-2-phenyl-ethyl)-amide

HRID 1189091
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HRID 1189091 반응식
[OH:1][CH:2]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH2:3][NH:4][C:5](=[O:10])[CH2:6][CH2:7][C:8]#[CH:9].C1C=C[NH+]=CC=1.[O-][Cr](Cl)(=O)=O>C(Cl)Cl>[O:1]=[C:2]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[CH2:3][NH:4][C:5](=[O:10])[CH2:6][CH2:7][C:8]#[CH:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 86086915N-(2-hydroxy-2-phenylethyl)pent-4-ynamideHCID 178418287HCID 178418287, 화합물

생성물 1

HCID 86086916Pent-4-ynoic acid (2-oxo-2-phenyl-ethyl)-amide수율 95%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

169 mg (0.78 mmol) of N-(2-hydroxy-2-phenylethyl)pent-4-ynamide in DCM (1 mL) were added to a solution of PCC (326 mg, 1.48 mmol) in DCM (4 mL). The reaction mixture was stirred for 4 hours at room temperature, dissolved in DCM and then quenched with NaOH 1N. The organic phase was washed with brine, dried over MgSO4, filtered and concentrated to yield 160 mg (0.74 mmol, 95%) of pent-4-ynoic acid (2-oxo-2-phenyl-ethyl)-amide as a yellow solid.

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후처리

  1. customquenched with NaOH 1N
  2. washThe organic phase was washed with brine
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-d3c2dbf7501c4a2db9fc40356b048767
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08674106B2

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