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Hydrochloric Acid → 5-(Dimethylamino)-N-(2-oxoethyl)naphthalene-1-sulfonamide

HRID 926233
ノート
印刷プレビュー

反応式

HRID 926233 の反応式
C[O:2][CH:3](OC)[CH2:4][NH:5][S:6]([C:9]1[C:18]2[C:13](=[C:14]([N:19]([CH3:21])[CH3:20])[CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7].Cl>CO>[O:2]=[CH:3][CH2:4][NH:5][S:6]([C:9]1[C:18]2[C:13](=[C:14]([N:19]([CH3:21])[CH3:20])[CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 84426875HCID 84426875、化合物

生成物 1

HCID 187021755-(Dimethylamino)-N-(2-oxoethyl)naphthalene-1-sulfonamide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
25 °C

実験手順

The acetal 11 (287 mg, 850 mop was dissolved in MeOH (1 mL) and coned HCl (0.5 mL) was added to the solution, which was stirred for 1 h at 25° C. The reaction mixture was then evaporated to dryness; the material left was dissolved in CH2Cl2 (10 mL) and the solution was washed with NaHCO3 (2 mL of a saturated aqueous solution). The organic layer was collected and was evaporated under low pressure to give the aldehyde as a light green foam, the total amount of which was used without further purification in the preparation of 12.

後処理

  1. customThe reaction mixture was then evaporated to dryness
  2. waitthe material left
  3. dissolutionwas dissolved in CH2Cl2 (10 mL)
  4. washthe solution was washed with NaHCO3 (2 mL of a saturated aqueous solution)
  5. customThe organic layer was collected
  6. customwas evaporated under low pressure

出典と根拠

ORDレコード
ord-615ea1dead5a42e0b63008c3fd082021
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09284343B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート