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Ammonium Carbonate → 2-(2-Iodophenyl)acetamide

HRID 1778951
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HRID 1778951 반응식
[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=O.C(=O)([O-])[O-].[NH4+:16].[NH4+]>S(Cl)(Cl)=O>[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([NH2:16])=[O:11]
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참가 물질

4

반응물 2

HCID 517111Ammonium CarbonateHCID 27800902-Iodophenylacetic acid

생성물 1

HCID 184740882-(2-Iodophenyl)acetamide

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

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온도
60 °C

실험 절차

A solution of 2-iodophenylacetic acid (20.5 g, 78.2 mmol) in thionyl chloride (70 mL) was stirred at 75° C. for 3 hours. The thionyl chloride was removed in vacuo and the resulting residue was dissolved in DCM (100 mL). Ammonium carbonate (15.03 g, 156.5 mmol) was added and the resulting mixture was stirred at 60° C. for 20 hours. The volatiles were evaporated in vacuo, water (100 mL) was added and the resulting suspension was sonicated for 1 minute, before filtering and washing the filter cake with water then Et2O. After air drying, the title compound I6 was obtained as a light cream coloured solid (12.9 g, 63%); 1H NMR (300 MHz, d6-DMSO) δ 7.82 (d, J=8.3 Hz, 1H), 7.41 (brs s, 1H), 7.30-7.37 (m, 2H), 6.95-7.01 (m, 2H), 3.55 (s, 2H). LCMS-B: rt 5.108 min; m/z 262 [M+H]+.

후처리

  1. customThe thionyl chloride was removed in vacuo
  2. dissolutionthe resulting residue was dissolved in DCM (100 mL)
  3. customThe volatiles were evaporated in vacuo, water (100 mL)
  4. additionwas added
  5. customthe resulting suspension was sonicated for 1 minute
  6. filtrationbefore filtering
  7. washwashing the filter cake with water
  8. customAfter air drying

출처 및 근거

ORD 기록
ord-c5fa446c69f6416cac348e2f004e729e
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09266864B2

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