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O-Methylhydroxylamine hydrochloride → (4E)-N-Methoxy-6-methyl-3,4-dihydro-2H-1-benzopyran-4-imine

HRID 1662139
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HRID 1662139 반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][CH2:7][CH2:6][C:5]2=O.Cl.[O:14]([NH2:16])[CH3:15]>N1C=CC=CC=1>[CH3:15][O:14][N:16]=[C:5]1[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([CH3:1])[CH:3]=2)[O:8][CH2:7][CH2:6]1
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참가 물질

4

반응물 2

HCID 521874O-Methylhydroxylamine hydrochlorideHCID 5843546-Methyl-4-chromanone

생성물 1

HCID 86605441(4E)-N-Methoxy-6-methyl-3,4-dihydro-2H-1-benzopyran-4-imine

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

6-Methylchroman-4-one (Aldrich, 3.24 g, 20 mmol) was dissolved in pyridine (15 mL). Methoxylamine hydrochloride (1.84 g, 22 mmol) was added and the mixture stirred for 16 hours at ambient temperature. The pyridine was removed under reduced pressure, and the residue was added to water and diethyl ether. The aqueous layer was extracted with diethyl ether, and the combined organic layers washed with 1N sodium hydroxide and 1N hydrochloric acid and then dried with magnesium sulfate and filtered. The solvent was removed under reduced pressure to afford the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 2.28 (s, 3H), 2.88 (t, J=6.27 Hz, 2H), 3.98 (s, 3H), 4.17 (t, J=6.27 Hz, 2H), 6.78 (d, J=8.48 Hz, 1H), 7.05 (dd, J=8.48, 2.03 Hz, 1H), 7.70 (d, J=2.03 Hz, 1H). MS (DCI) m/z 192.02 (M+H)+.

후처리

  1. customThe pyridine was removed under reduced pressure
  2. additionthe residue was added to water and diethyl ether
  3. extractionThe aqueous layer was extracted with diethyl ether
  4. washthe combined organic layers washed with 1N sodium hydroxide and 1N hydrochloric acid
  5. dry with materialdried with magnesium sulfate
  6. filtrationfiltered
  7. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-6e026e57cfc34dc691eb7ccf665896a3
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08030504B2

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