Hydroxylamine HCl → 2-Chloro-3-hydroxybenzonitrile

HRID 222338

반응식

HRID 222338 반응식
[Cl:1][C:2]1[C:9]([OH:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[Cl-].O[NH3+:13]>C(O)(=O)C.C(OCC)(=O)C>[Cl:1][C:2]1[C:9]([OH:10])=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:13]

참가 물질

5

반응물 2

HCID 21645Hydroxylamine HClHCID 5933762-Chloro-3-hydroxybenzaldehyde

생성물 1

HCID 214365452-Chloro-3-hydroxybenzonitrile

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 2-chloro-3-hydroxybenzaldehyde [(2 g, 12.8 mmol) WO 2005007633, p 34] and hydroxylammonium chloride (1.33 g, 19.6 mmol) in acetic acid (20 mL) was heated under reflux for 2 hours. The reaction mixture was then cooled to room temperature and partitioned between diethyl ether and water. The organic layer was separated, washed with brine, dried over magnesium sulfate and concentrated in vacuo to give a white solid. The solid was then dissolved in ethyl acetate washed with water and brine, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a solid in quantitative yield.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hours
  3. custompartitioned between diethyl ether and water
  4. customThe organic layer was separated
  5. washwashed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customto give a white solid
  9. washwashed with water and brine
  10. dry with materialdried over magnesium sulfate
  11. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3228a409c4a9446ebecc30f3b3fc2962
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08207198B2

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