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HCID 29544554、化合物 → HCID 70197765、化合物

HRID 1626968
ノート
印刷プレビュー

反応式

HRID 1626968 の反応式
[CH:1]1([CH2:4][NH:5][C:6]2[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[CH:8][C:7]=2[N+:14]([O-])=O)[CH2:3][CH2:2]1>C(O)C>[CH:1]1([CH2:4][NH:5][C:6]2[C:7]([NH2:14])=[CH:8][C:9]([O:12][CH3:13])=[CH:10][CH:11]=2)[CH2:2][CH2:3]1
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

3

反応物 1

HCID 29544554HCID 29544554、化合物

生成物 1

HCID 70197765HCID 70197765、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
10 °C

実験手順

N-(Cyclopropylmethyl)-4-methoxy-2-nitroaniline (175 g) was dissolved in ethanol (1750 mL) and added to a 4.0 L Hast ‘C’ Shaker can. The mixture was cooled to 10° C. and treated with 3% Pt/0.6% VG/C, deGussa (4.5 g). The vessel was sparged under nitrogen and then sparged three times with hydrogen at a setting of 40 psi and agitated for 2.5 hours. To a pre-washed solka-flok with ethanol, the reaction mixture was filtered through solka-flok through a sintered glass funnel to have about a ½ inch depth of solka-flok. The solka -flok was then washed with 1 L ethanol and concentrated in vacuo, providing the titled compound.

後処理

  1. additionadded to a 4.0 L Hast ‘C’ Shaker can
  2. customThe vessel was sparged under nitrogen
  3. customsparged three times with hydrogen at a setting of 40 psi
  4. filtrationTo a pre-washed solka-flok with ethanol, the reaction mixture was filtered through solka-flok through a sintered glass funnel
  5. washThe solka -flok was then washed with 1 L ethanol
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-9fb7de96a79a446186fe1b342352fb1d
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785481B2

反応ノート

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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