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Ammonium Hydroxide → 3-Iodo-4-methylbenzamide

HRID 1619132
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HRID 1619132 반응식
Cl.C[N:3](C)CCCN=C=NCC.O.N1(O)C2C=CC=CC=2N=N1.[OH-].[NH4+].[I:26][C:27]1[CH:28]=[C:29]([CH:33]=[CH:34][C:35]=1[CH3:36])[C:30](O)=[O:31]>CN(C=O)C>[I:26][C:27]1[CH:28]=[C:29]([CH:33]=[CH:34][C:35]=1[CH3:36])[C:30]([NH2:3])=[O:31]
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참가 물질

6

반응물 4

HCID 14923Ammonium HydroxideHCID 6216403-Iodo-4-methylbenzoic acidHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrate

생성물 1

HCID 8333293-Iodo-4-methylbenzamide수율 87%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.49 g, 28.6 mmol), 1H-benzo[d][1,2,3]triazol-1-ol hydrate (3.90 g, 28.9 mmol) and 32% aqueous ammonium hydroxide solution (1.10 mL, 28.7 mmol) were sequentially added to a stirred solution of 3-iodo-4-methylbenzoic acid (5.00 g, 19.1 mmol) in N,N′-dimethylformamide (15 mL) at room temperature. After stirring overnight, the mixture was concentrated in vacuo and water and dichloromethane were added to the mixture. The organic layer was washed with 2N aqueous sodium hydroxide solution, brine, dried (MgSO4) and evaporated to give the title compound (4.34 g, 70%) as a yellow solid.

후처리

  1. concentrationthe mixture was concentrated in vacuo and water and dichloromethane
  2. additionwere added to the mixture
  3. washThe organic layer was washed with 2N aqueous sodium hydroxide solution, brine
  4. dry with materialdried (MgSO4)
  5. customevaporated

출처 및 근거

ORD 기록
ord-f45e531ea34f4ed4a834b05c1e81714b
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772288B2

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