Hydroxylamine HCl → 4-Hydroxy-3-methylbenzonitrile

HRID 225819노트

반응식

HRID 225819 반응식
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=1[CH3:10].[Cl-].O[NH3+:13]>C(O)(=O)C.C(OCC)C>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:13])=[CH:4][C:3]=1[CH3:10]

참가 물질

5

반응물 2

HCID 21645Hydroxylamine HClHCID 1399014-Hydroxy-3-methylbenzaldehyde

생성물 1

HCID 109645604-Hydroxy-3-methylbenzonitrile수율 66%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 3283Diethyl Ether용매

실험 절차

A mixture of 4-hydroxy-3-methylbenzaldehyde (530 mg, 3.91 mmol) and hydroxyl ammonium chloride (406 mg, 5.81 mmol) in acetic acid (5 mL) was heated under reflux for 90 minutes. The cooled reaction mixture was then diluted with diethyl ether (30 mL) and washed with water (30 mL). The combined organic solution was washed with brine, dried over magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol, 100:0 to 97.5:2.5, to afford the title compound as a pale yellow oil in 66% yield, 345 mg.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 90 minutes
  3. customThe cooled reaction mixture
  4. washwashed with water (30 mL)
  5. washThe combined organic solution was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customthe residue was purified by column chromatography on silica gel
  9. washeluting with dichloromethane

출처 및 근거

ORD 기록
ord-b8f1e8a279104573b4de025a7e89a728
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07557131B2

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