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Hydrochloric Acid → HCID 57577379、化合物

HRID 1921689
ノート
印刷プレビュー

反応式

HRID 1921689 の反応式
C([O:3][C:4](=[O:33])[C:5]([NH:29]C(=O)C)([CH:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH:17]=2)[CH2:12]1)C(OCC)=O)C.Cl>CO>[NH2:29][CH:5]([CH:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH:17]=2)[CH2:12]1)[C:4]([OH:33])=[O:3]
参加物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 57577378Diethyl 2-acetamido-2-(6-octyl-1,2,3,4-tetrahydronaphthalen-2-yl)malonate

生成物 1

HCID 57577379HCID 57577379、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Compound 6 (300 mg, 0.65 mmol) was added to 12 M HCl (10 ml). The mixture was heated to reflux and MeOH (5 ml) was added until the mixture became homogenous. Reflux was continued for 2 hours until the starting material was consumed as determined by thin layer chromatography (TLC). The reaction mixture was concentrated under reduced pressure and co-evaporated with MeOH and diethyl ether multiple times. The desired compound 8 was recrystallized from diethyl ether and hexanes to provide a light brown solid and used directly for the next reaction.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux
  3. temperatureReflux
  4. customwas consumed
  5. concentrationThe reaction mixture was concentrated under reduced pressure and co-evaporated with MeOH and diethyl ether multiple times
  6. customThe desired compound 8 was recrystallized from diethyl ether and hexanes
  7. customto provide a light brown solid
  8. customused directly for the next reaction

出典と根拠

ORDレコード
ord-19ae8d4985514383ab9ca3a742c9d39b
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08173710B2

反応ノート

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