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Nitric Acid → (4-Hydroxy-3-nitro-phenoxy)-acetonitrile

HRID 1106731
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인쇄 미리보기

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HRID 1106731 반응식
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([O:6][CH2:7][C:8]#[N:9])=[CH:4][CH:3]=1.[N+:12]([O-])([OH:14])=[O:13].C(OCC)(=O)C>[N+](C)([O-])=O>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][C:8]#[N:9])=[CH:10][C:11]=1[N+:12]([O-:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 8857Ethyl AcetateHCID 137506092-(4-Hydroxyphenoxy)acetonitrile

생성물 1

HCID 18789604(4-Hydroxy-3-nitro-phenoxy)-acetonitrile

시약·촉매·용매 1

HCID 6375Nitromethane용매

실험 절차

A solution of 7.5 g of (4-hydroxy-phenoxy)-acetonitrile dissolved in 60 ml of nitromethane was cooled in an ice bath and 3.88 ml of 70% nitric acid was added dropwise. After 45 minutes, the reaction mixture was poured into ethyl acetate, washed with brine, dried (MgSO4), and evaporated to dryness. The crude product was purified by silica gel chromatography eluting with ethyl acetate/hexane (1:3), giving 5.45 g of (4-hydroxy-3-nitro-phenoxy)-acetonitrile as a yellow solid, mp 113.1-114.1° C.

후처리

  1. temperaturewas cooled in an ice bath
  2. washwashed with brine
  3. dry with materialdried (MgSO4)
  4. customevaporated to dryness
  5. customThe crude product was purified by silica gel chromatography
  6. washeluting with ethyl acetate/hexane (1:3)

출처 및 근거

ORD 기록
ord-48ac53ddc23e452e8daf701e553c2682
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057349

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