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Sodium Hydroxide → 3-(Methanesulfonylmethyl)aniline

HRID 1405170
ノート
印刷プレビュー

反応式

HRID 1405170 の反応式
[CH3:1][S:2]([CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-])=O)[CH:7]=1)(=[O:4])=[O:3].[OH-].[Na+]>Cl.C1COCC1.[Cl-].[Ti+3].[Cl-].[Cl-]>[CH3:1][S:2]([CH2:5][C:6]1[CH:7]=[C:8]([CH:9]=[CH:10][CH:11]=1)[NH2:12])(=[O:3])=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 14798Sodium HydroxideHCID 179084331-(Methanesulfonylmethyl)-3-nitrobenzene

生成物 1

HCID 219563393-(Methanesulfonylmethyl)aniline収率 102.1%

試薬・触媒・溶媒 3

HCID 10313229titanium(III) trichloride触媒HCID 313Hydrochloric Acid溶媒HCID 8028
Tetrahydrofuran
溶媒

実験手順

Titanium(III)chloride solution (about 15%) in about 10% hydrochloric acid (MERCK (MDA) INCL SCHUCHARDT, 162 ml) was added to a stirred solution of 1-[(methylsulfonyl)methyl]-3-nitrobenzene (5.1 g; 23.8 mmol) in THF (250 ml) at room temperature and the batch was stirred for 16 hours. By adding 1N sodium hydroxide solution the pH value of the reaction mixture was raised to 10 before the batch was extracted with ethyl acetate (2×). The combined organic phases were washed with brine, filtered using a Whatman filter and concentrated to give the desired product (4.5 g) that was used without further purification.

後処理

  1. temperaturewas raised to 10 before the batch
  2. extractionwas extracted with ethyl acetate (2×)
  3. washThe combined organic phases were washed with brine
  4. filtrationfiltered
  5. filtrationfilter
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-a786e88c09fc444891563fdf22593510
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08916557B2

反応ノート

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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