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Hydroxyamine hydrochloride → HCID 76779877, 화합물

HRID 1049094
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HRID 1049094 반응식
[C:1]([C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][C:5]=1[CH3:14])(=O)[CH3:2].Cl.[NH2:16][OH:17].C([O-])(=O)C.[Na+]>CO>[OH:17][N:16]=[C:1]([C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][C:5]=1[CH3:14])[CH3:2]
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참가 물질

5

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 20665294Methyl 4-acetyl-3-methylbenzoate

생성물 1

HCID 76779877HCID 76779877, 화합물수율 100.1%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
40 °C

실험 절차

Methyl 4-acetyl-3-methylbenzoate (1.49 g, 7.76 mmol), hydroxylamine hydrochloride (4.18 g, 60.1 mmol), and sodium acetate (4.93 g, 60.1 mmol) were suspended in methanol (40 mL) and the reaction mixture heated at 40° C. for 2 h. Upon cooling to room temperature the solvent was removed under reduced pressure. The residue obtained was partitioned between ethyl acetate (75 mL) and water (30 mL). The organic extract was washed with water (20 mL) and brine. The washed extract was dried over sodium sulfate, filtered and concentrated under reduced pressure to afford the title compound as a solid (1.61 g, 100%). LC-MS: (FA) ES+ 208; 1H NMR (300 MHz, MeO D) δ 7.91-7.77 (m, 2H), 7.31 (d, J=8.0 Hz, 0.7H), 7.16 (d, J=7.9 Hz, 0.3H), 3.89 (s, 3H), 2.37 (s, 2H), 2.28 (s, 1H), 2.17 (s, 2H), 2.10 (s, 1H).

후처리

  1. temperatureUpon cooling to room temperature the solvent
  2. customwas removed under reduced pressure
  3. customThe residue obtained
  4. customwas partitioned between ethyl acetate (75 mL) and water (30 mL)
  5. extractionThe organic extract
  6. washwas washed with water (20 mL) and brine
  7. extractionThe washed extract
  8. dry with materialwas dried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e158915b1b22449595063aabda18a7b3
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09382197B2

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