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Acetic Acid → 2-Amino-4-fluoro-6-methylbenzonitrile

HRID 17549
ノート
印刷プレビュー

反応式

HRID 17549 の反応式
C(O)(=O)C.Cl.O.O.[Sn](Cl)(Cl)(Cl)Cl.[F:13][C:14]1[CH:21]=[C:20]([N+:22]([O-])=O)[C:17]([C:18]#[N:19])=[C:16]([CH3:25])[CH:15]=1.[OH-].[Na+]>CO>[NH2:22][C:20]1[CH:21]=[C:14]([F:13])[CH:15]=[C:16]([CH3:25])[C:17]=1[C:18]#[N:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 544206034-Fluoro-2-methyl-6-nitrobenzonitrileHCID 85782573Tin tetrachloride dihydrate

生成物 1

HCID 450790392-Amino-4-fluoro-6-methylbenzonitrile収率 104.9%

試薬・触媒・溶媒 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
HCID 887
Methanol
溶媒

実験手順

Acetic acid (16.0 ml, 28 mmol) was added to a concentrated hydrochloric acid (90 ml) solution of tin chloride dihydrate (63.1 g, 280 mmol), and 4-fluoro-2-methyl-6-nitrobenzonitrile (I-263) (16.8 g, 93.3 mmol) was added, then methanol (8 ml) was added. Since the reaction liquid greatly generated heat, it was cooled with ice. After stirring for 1 hour, the reaction mixture liquid was poured into aqueous sodium hydroxide solution (4.6 M, 500 ml) with ice therein. The precipitated solid was collected by filtration, washed with water, then dried to obtain the entitled compound (14.7 g, 99%) as a gray solid.

後処理

  1. additionwas added
  2. customSince the reaction liquid
  3. temperaturegreatly generated heat
  4. temperatureit was cooled with ice
  5. filtrationThe precipitated solid was collected by filtration
  6. washwashed with water
  7. customdried

出典と根拠

ORDレコード
ord-234628892ac14dcf83801d1683fe9b29
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07737166B2

反応ノート

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