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Hydrazine hydrate (1:1) → (4,5-Dichlorothiophen-2-yl)methanamine

HRID 844010
ノート
印刷プレビュー

反応式

HRID 844010 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:8][N:9]2C(=O)C3C(=CC=CC=3)C2=O)[S:5][C:6]=1[Cl:7].O.NN>CO.O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:8][NH2:9])[S:5][C:6]=1[Cl:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 226120382-(4,5-Dichloro-thiophen-2-ylmethyl)-isoindole-1,3-dione

生成物 1

HCID 22612362(4,5-Dichlorothiophen-2-yl)methanamine収率 75.8%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred suspension of 2-(4,5-Dichloro-thiophen-2-ylmethyl)-isoindole-1,3-dione (0.770 grams, 2.47 mmole) in methanol (30 ml) and tetrahydrofuran (10 ml) at room temperature was added hydrazine hydrate (0.395 grams, 12.3 mmole) and stirred at room temperature over night. A precipitate formed, and the mixture was concentrated to about 15 ml and filtered. The filtrate was poured into 100 ml water and extracted with diethyl ether. The combined extracts were washed with water and brine, dried over MgSO4, filtered, and concentrated to an oil which was purified via flash chromatography on silica using 5% methanol/methylene chloride as eluent to give an oil (0.341 g). MW 182.08; MS (m/e) 183 (M++1).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customA precipitate formed
  2. concentrationthe mixture was concentrated to about 15 ml
  3. filtrationfiltered
  4. additionThe filtrate was poured into 100 ml water
  5. extractionextracted with diethyl ether
  6. washThe combined extracts were washed with water and brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated to an oil which
  10. customwas purified via flash chromatography on silica using 5% methanol/methylene chloride as eluent

出典と根拠

ORDレコード
ord-d2a8beefc9fb46f6938be6db1523dca5
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06380218B1

反応ノート

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