O-[(5-chlorothiophen-2-yl)methyl]hydroxylamine → HCID 136127206, Verbindung

HRID 621370Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 621370
[C:1]([C:4]1[C:5](=[O:17])[CH2:6][CH:7]([CH:11]2[CH2:16][CH2:15][CH2:14][S:13][CH2:12]2)[CH2:8][C:9]=1[OH:10])(=O)[CH3:2].[Cl:18][C:19]1[S:23][C:22]([CH2:24][O:25][NH2:26])=[CH:21][CH:20]=1>C(O)C>[Cl:18][C:19]1[S:23][C:22]([CH2:24][O:25][N:26]=[C:1]([C:4]2[C:5](=[O:17])[CH2:6][CH:7]([CH:11]3[CH2:16][CH2:15][CH2:14][S:13][CH2:12]3)[CH2:8][C:9]=2[OH:10])[CH3:2])=[CH:21][CH:20]=1

Komponenten

4

Versuchsvorschrift

A solution containing 5.1 g (0.020 mol) of 2-acetyl-3-hydroxy-5-(tetrahydro-2H-thiopyran-3-yl)cyclohex-2-en-1-one and 3.4 g (0.021 mol) of (5-chlorothien-2-yl)methoxyamine in 200 ml of ethanol was stirred overnight (about 14 hours) at room temperature and then evaporated to remove ethanol. The concentrate was diluted with 150 ml of methylene chloride and then washed with 100 ml of water and then with 100 ml of saturated aqueous sodium chloride solution. The washed methylene chloride solution was dried over anhydrous magnesium sulfate and then evaporated to dryness under reduced pressure to afford a white solid. Recrystallation of this solid with absolute ethanol afforded 7.6 g of the title compound, m.p. 154°-155° C. cl EXAMPLE 2

Aufarbeitung

  1. customevaporated
  2. customto remove ethanol
  3. additionThe concentrate was diluted with 150 ml of methylene chloride
  4. washwashed with 100 ml of water
  5. dry with materialThe washed methylene chloride solution was dried over anhydrous magnesium sulfate
  6. customevaporated to dryness under reduced pressure
  7. customto afford a white solid

Quellen und Nachweise

ORD-Eintrag
ord-14a32d15285245cc88b0fdf6fbdb98ff
Quelldatensatz
uspto-grants-1989_04
Patentnummer
US04824470

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