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Acetic Anhydride → N-(4-cyano-2-iodophenyl)acetamide

HRID 1018788
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HRID 1018788 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[I:10].[C:11](OC(=O)C)(=[O:13])[CH3:12]>S(=O)(=O)(O)O.O>[C:11]([NH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[I:10])(=[O:13])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7918Acetic AnhydrideHCID 44163954-Amino-3-iodobenzonitrile

생성물 1

HCID 22991943N-(4-cyano-2-iodophenyl)acetamide수율 95%

시약·촉매·용매 2

HCID 1118Sulfuric Acid촉매HCID 962Water용매

실험 절차

A mixture of 8.54 g (0.035 mole) of 4-amino-3-iodobenzonitrile (31), 16 mL (16.32 g, 0.16 mole) of acetic anhydride and five drops of concentrated sulfuric acid was heated at 700 under reflux for 10 minutes (the mixture became thick when the temperature reached 400 and some manual stirring was required). The reaction mixture was poured over 400 mL of cold water and stirred for 5 minutes to give a white solid which was filtered and dried, yielding 9.48 g (95%) of 32 as white powder, mp 176-181°. Infrared (IR) and NMR analysis gave the following results: IR (potassium bromide): 3276 (NH), 2230 (CN), 1663 (C=O), 1517, 1297 cm−1. 1H nmr (90 MHz, CDCI3):δ 8.73 (1H, br s, NH), 8.13-8.05 (2H, m, H-5 and H-2), 7.65 (1 H; dd, 3JH5-H6=8.4 Hz, 4JH2-H6=1.8 Hz; H-6), 2.25 (3H, s, CH3).

후처리

  1. temperaturewas heated at 700
  2. temperatureunder reflux for 10 minutes (the mixture
  3. stirringstirred for 5 minutes
  4. customto give a white solid which
  5. filtrationwas filtered
  6. customdried

출처 및 근거

ORD 기록
ord-2b2caf05ec204e249163895b844ccc2a
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06482982B1

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