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Formaldehyde → N-(Hydroxymethyl)phenylacetamide

HRID 2427925
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HRID 2427925 반응식
[C:1]1([CH2:7][C:8]([NH2:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:11]=[O:12]>C(=O)([O-])[O-].[K+].[K+]>[OH:12][CH2:11][NH:10][C:8](=[O:9])[CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 712FormaldehydeHCID 7680Benzeneacetamide

생성물 1

HCID 138717N-(Hydroxymethyl)phenylacetamide수율 44.4%

시약·촉매·용매 1

HCID 11430Potassium Carbonate촉매

실험 절차

A mixture of phenylacetamide 12 (2 g, 15 mmol) in a solution of potassium carbonate (4%, 2 ml, 0.6 mmol) and an aqueous solution of formaldehyde (37%, 2 ml, 20 mmol) was refluxed for 15 min (until completely dissolved). The mixture was cooled and extracted with CH2Cl2 (2×30 ml). The combined organic phases were dried over MgSO4 and were concentrated under reduced pressure to give a crude product (1.35 g), recrystallization in toluene (20 ml) gave N-hydroxymethylphenylacetamide 11 (1.1 g, 44%) in the form of a white powder. M.p. 78° C. 1H NMR (CDCl3, 300 MHz) δ 7.50-7.20 (m, 5H), 6.48 (br s, NH), 4.69 (t, J=7.0 Hz, 2H), 3.67 (t, J=7 Hz, OH), 3.60 (s, 2H). 13C NMR (CDCl3, 75 MHz) δ 172.9, 134.4, 129.5, 129.0, 127.5, 64.2, 43.6.

후처리

  1. dissolutionuntil completely dissolved)
  2. temperatureThe mixture was cooled
  3. extractionextracted with CH2Cl2 (2×30 ml)
  4. dry with materialThe combined organic phases were dried over MgSO4
  5. concentrationwere concentrated under reduced pressure
  6. customto give
  7. customa crude product (1.35 g), recrystallization in toluene (20 ml)

출처 및 근거

ORD 기록
ord-9beed3ec75f04d538e87fc4ff7e16c0c
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968735B2

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