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Sodium Hydroxide → 6-Iodobenzo[d][1,3]dioxol-5-amine

HRID 1476727
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HRID 1476727 반응식
[I:1][C:2]1[C:3]([NH:11]C(=O)C)=[CH:4][C:5]2[O:9][CH2:8][O:7][C:6]=2[CH:10]=1.[OH-].[Na+]>C(O)C.O>[I:1][C:2]1[C:3]([NH2:11])=[CH:4][C:5]2[O:9][CH2:8][O:7][C:6]=2[CH:10]=1
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 53488067N-(6-Iodo-2H-1,3-benzodioxol-5-yl)acetamide

생성물 1

HCID 534880686-Iodobenzo[d][1,3]dioxol-5-amine수율 98.5%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

A solution of N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide (200 mg, 0.656 mmol) and NaOH (1.31 g, 32.8 mmol) in ethanol (26 mL) and water (6 mL) was heated to reflux with stirring for 4 h. The mixture was cooled and the solvent was removed under vacuum. The residue was partitioned between methylene chloride (100 mL) and water (100 mL). The organic layer was washed with water (2×100 mL), dried (MgSO4) and evaporated under vacuum to give 6-iodobenzo[d][1,3]dioxol-5-amine (170 mg, 98%) as orange solid. LCMS: 264 [M+1]+; 1H NMR (DMSO-d6) δ 4.88 (s, 2H), 5.87 (s, 2H), 6.47 (s, 1H), 7.07 (s, 1H).

후처리

  1. temperatureto reflux
  2. temperatureThe mixture was cooled
  3. customthe solvent was removed under vacuum
  4. customThe residue was partitioned between methylene chloride (100 mL) and water (100 mL)
  5. washThe organic layer was washed with water (2×100 mL)
  6. dry with materialdried (MgSO4)
  7. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-8b74519ed7674fdcb4087268b86d389e
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09402832B2

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