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Trifluoroacetic acid → 3-Aminomethyl-5-chloro-4-fluoro-benzonitrile

HRID 1527475
ノート
印刷プレビュー

反応式

HRID 1527475 の反応式
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[C:13]([C:15]#[N:16])[CH:12]=[C:11]([Cl:17])[C:10]=1[F:18])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH2:7][CH2:8][C:9]1[CH:14]=[C:13]([CH:12]=[C:11]([Cl:17])[C:10]=1[F:18])[C:15]#[N:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 68283962(3-Chloro-5-cyano-2-fluoro-benzyl)-carbamic acid tert-butyl ester

生成物 1

HCID 682834833-Aminomethyl-5-chloro-4-fluoro-benzonitrile

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of (3-chloro-5-cyano-2-fluoro-benzyl)-carbamic acid tert-butyl ester (645 mg, 2.27 mmol) in CH2Cl2 (15 mL) was added TFA (1.75 mL, 22.7 mmol), and stirring was continued at RT overnight. Volatiles were removed under reduce pressure, water was added and the mixture was washed with EtOAc. The aqueous layer was basified to pH=12 by addition of 4M NaOH solution and extracted twice with EtOAc. The combined organics were dried (phase separator) and evaporated to afford the title compound as a beige solid. MS (LC/MS): 185.0 [M+H]+; tR (HPLC conditions c): 2.62 min.

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. customVolatiles were removed
  2. additionwas added
  3. washthe mixture was washed with EtOAc
  4. additionThe aqueous layer was basified to pH=12 by addition of 4M NaOH solution
  5. extractionextracted twice with EtOAc
  6. customThe combined organics were dried (phase separator)
  7. customevaporated

出典と根拠

ORDレコード
ord-7ae8cd0958a2440cac83ab203cc94379
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09085555B2

反応ノート

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