5,6-Dinitro-1,3-benzodioxole → 6-Nitro-1,3-benzodioxol-5-amine

HRID 577612

반응식

HRID 577612 반응식
[N+:1]([C:4]1[C:12]([N+:13]([O-])=O)=[CH:11][C:7]2[O:8][CH2:9][O:10][C:6]=2[CH:5]=1)([O-:3])=[O:2]>C(O)(=O)C>[N+:1]([C:4]1[C:12]([NH2:13])=[CH:11][C:7]2[O:8][CH2:9][O:10][C:6]=2[CH:5]=1)([O-:3])=[O:2]

참가 물질

3

반응물 1

HCID 6113255,6-Dinitro-1,3-benzodioxole

생성물 1

HCID 6026656-Nitro-1,3-benzodioxol-5-amine수율 84.4%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

Compound 5,6-dinitrobenzo[d][1,3]dioxole (6.0 g, 28.3 mmol) was added to stirred glacial acetic acid (120 mL) under N2 atmosphere. After the mixture was heated to boiling, the heat source was removed and iron powder (4.75 g) added with vigorous stirring. Quick spontaneous boiling occurred, the mixture turned dark and the exothermic reaction subsided (2-5 min). The mixture was refluxed for 10 min and poured into ice/water. The orange-red product was isolated by filtration, dissolved in glacial acetic acid, and the solution filtered while hot. The filtrate was poured into ice-cold water. The orange-red solid product was isolated by filtration and dried to provide compound 6-nitrobenzo[d][1,3]dioxol-5-amine (4.35 g, 84%). LCMS: 183 [M+1]+; 1H NMR (DMSO-d6) δ 6.06 (s, 2H), 6.51 (s, 1H), 7.36 (s, 1H), 7.73 (s, 2H).

후처리

  1. temperatureAfter the mixture was heated
  2. customthe heat source was removed
  3. additioniron powder (4.75 g) added with vigorous stirring
  4. customthe exothermic reaction
  5. custom(2-5 min)
  6. temperatureThe mixture was refluxed for 10 min
  7. customThe orange-red product was isolated by filtration
  8. filtrationthe solution filtered while hot
  9. additionThe filtrate was poured into ice-cold water
  10. customThe orange-red solid product was isolated by filtration
  11. customdried

출처 및 근거

ORD 기록
ord-6e6029a8c7c24decb7ed0e385748c29e
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09040556B2

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