Hydroxyamine hydrochloride → HCID 86753147, compound

HRID 2395144Notes

Reaction equation

HRID 2395144 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:7]([CH3:27])([CH3:26])[C:8]3[C:13]([O:14][C:15]=2[C:16]=1[CH2:17][C:18]([O:20][CH3:21])=[O:19])=[C:12]([CH:22]=O)[C:11]([O:24][CH3:25])=[CH:10][CH:9]=3.C([O-])(=O)C.[Na+].Cl.[NH2:34][OH:35]>CO.C1COCC1.O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:7]([CH3:27])([CH3:26])[C:8]3[C:13]([O:14][C:15]=2[C:16]=1[CH2:17][C:18]([O:20][CH3:21])=[O:19])=[C:12]([CH:22]=[N:34][OH:35])[C:11]([O:24][CH3:25])=[CH:10][CH:9]=3

Participants

7

Procedure

5 g (13.5 mmol) of methyl 3,6-dimethoxy-9,9-dimethyl-5-formylxanthene-4-acetate were dissolved in a mixture of 75 ml of methanol, 75 ml of THF and 20 ml of water. After the addition of 1.66 g of sodium acetate and 1.4 g of hydroxylamine hydrochloride the mixture was stirred at room temperature overnight and then diluted with 200 ml of water. The precipitated solid was filtered off, washed with water and dried, whereby 4.95 g of methyl 3,6-dimethoxy-9,9-dimethyl-5-[(hydroximino)methyl]xanthene-4-acetate were obtained as a white powder of m.p. 234°-236°; IR 1743, 1629, 1604, 1582, 1498 cm-1.

Workup

  1. filtrationThe precipitated solid was filtered off
  2. washwashed with water
  3. customdried

Sources & evidence

ORD record
ord-0284f2bcf45441f7904da78b13ca665a
Source dataset
uspto-grants-1998_09
Patent number
US05811548

Reaction notes

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