Hydrochloric Acid → HCID 178436837、化合物

HRID 1484476

反応式

HRID 1484476 の反応式
[OH:1][NH:2][C:3]([NH2:5])=[O:4].CO.CO[CH:10](OC)[CH2:11][C:12](=O)[CH2:13][CH3:14].C(O)C.[ClH:21]>>[ClH:21].[CH2:13]([C:12]1[N:5]=[C:3]([OH:4])[N+:2]([O-:1])=[CH:10][CH:11]=1)[CH3:14]

参加物

6

反応条件

温度
-6.5 °C

実験手順

0.388 mol (25.9 g) hydroxy urea were dissolved in 195 ml 2 M HCl, 80 ml of methanol were added and 0.388 mol (56.7 g) of 1,1-dimethoxypentane-3-on (62% content in product mixture) were added dropwise under cooling with the internal temperature being maintained at −6 to −7° C. The solution was thawed to room temperature in an ice bath and stirred for 1 h, then evaporated until dryness. The residue was suspended with 100 ml of acetone, the mixture was cooled to below 0° C. in an ice/ethanol bath, the solid filtered off and washed with little ice-cold acetone. After drying 32.6 g crude product were obtained. The crude product was heated until boiling with 200 ml ethanol, hot filtered and slowly cooled to −18° C. The precipitated solid was filtered off, washed with a little amount of ethanol and dried. 11.7 g of the title compound were obtained.

後処理

  1. temperatureunder cooling with the internal temperature
  2. customThe solution was thawed to room temperature in an ice bath
  3. customevaporated until dryness
  4. temperaturethe mixture was cooled to below 0° C. in an ice/ethanol bath
  5. filtrationthe solid filtered off
  6. washwashed with little ice-cold acetone
  7. dry with materialAfter drying 32.6 g crude product
  8. customwere obtained
  9. filtrationhot filtered
  10. temperatureslowly cooled to −18° C
  11. filtrationThe precipitated solid was filtered off
  12. washwashed with a little amount of ethanol
  13. customdried

出典と根拠

ORDレコード
ord-dcb726fdc3bb4008bcf77046605c0b12
出典データセット
uspto-grants-2016_08
特許番号
US09422247B2

関連ノート

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