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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Hydrochloric Acid → HCID 85826896、化合物

HRID 1254957
ノート
印刷プレビュー

反応式

HRID 1254957 の反応式
[C:1](OC)(=[O:3])C.[C:6](#[N:14])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[ClH:15].CC1CCCCC1>CO>[ClH:15].[C:6](=[NH:14])([O:3][CH3:1])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]
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

6

反応物 4

HCID 313Hydrochloric AcidHCID 6584Methyl AcetateHCID 7962MethylcyclohexaneHCID 31286Octanenitrile

生成物 1

HCID 85826896HCID 85826896、化合物収率 93.4%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

Methanol (2.81 g) and methyl acetate (30 ml) were added to octanenitrile (10.00 g), and the mixture was cooled to 0° C. Hydrogen chloride (7.50 g) was added and the mixture was stirred for 25 hours at the same temperature. Methylcyclohexane (60 ml) was added to the reaction solution, and then the solvent was distilled off under reduced pressure. Methylcyclohexane (20 ml) was added to the residue, the mixture was stirred for 1.5 hours at room temperature, and then crystals were filtered. The crystals were washed with methylcyclohexane and dried under reduced pressure to give the title compound as a white solid (14.45 g, 93.4% yield).

後処理

  1. distillationthe solvent was distilled off under reduced pressure
  2. additionMethylcyclohexane (20 ml) was added to the residue
  3. stirringthe mixture was stirred for 1.5 hours at room temperature
  4. filtrationcrystals were filtered
  5. washThe crystals were washed with methylcyclohexane
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-ea6a390f11f543fbae7d591a621f148f
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455659B2

反応ノート

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