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Hydrochloric Acid → 2-Fluoro-4-methylphenyl isothiocyanate

HRID 1008749
ノート
印刷プレビュー

反応式

HRID 1008749 の反応式
[C:1](Cl)(Cl)=[S:2].[F:5][C:6]1[CH:12]=[C:11]([CH3:13])[CH:10]=[CH:9][C:7]=1[NH2:8].C(N(CC)CC)C.Cl>C(Cl)(Cl)Cl>[F:5][C:6]1[CH:12]=[C:11]([CH3:13])[CH:10]=[CH:9][C:7]=1[N:8]=[C:1]=[S:2]
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 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 10040ThiophosgeneHCID 679842-Fluoro-4-methylaniline

生成物 1

HCID 27590302-Fluoro-4-methylphenyl isothiocyanate

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

Thiophosgen (4.0 mL) (supplied from Aldrich) was added dropwise to a solution of 2-fluoro-4-methylaniline (6.31 g) (supplied from Aldrich) in 70 mL of chloroform under ice cooling, and subsequently 15 mL of triethylamine was added dropwise thereto at the same temperature. The reaction solution was stirred at room temperature overnight. Then 70 mL of 1 N hydrochloric acid was added thereto, and the mixture was separated into two liquid phases. The organic layer was washed with 70 mL of water, dried on sodium sulfate anhydrate and subsequently concentrated The residue was applied onto the silica gel column and eluted with hexane, to yield 7.72 g of the title compound.

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. customthe mixture was separated into two liquid phases
  2. washThe organic layer was washed with 70 mL of water
  3. customdried on sodium sulfate anhydrate
  4. concentrationsubsequently concentrated The residue
  5. washeluted with hexane

出典と根拠

ORDレコード
ord-15855c07e4dc44bab118bb3abbf60819
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07973030B2

反応ノート

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