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2-Chloro-4-fluorophenylacetonitrile → Ammonia

HRID 494430
ノート
印刷プレビュー

反応式

HRID 494430 の反応式
[BH4-].[Na+].[Cl:3][C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:5]=1[CH2:11][C:12]#[N:13]>CO.O.O.O.O.O.O.[Co](Cl)Cl>[NH3:13].[Cl:3][C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:5]=1[CH2:11][CH2:12][NH2:13]
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 27250632-Chloro-4-fluorophenylacetonitrileHCID 4311764Sodium borohydride

生成物 2

HCID 222AmmoniaHCID 218881112-(2-Chloro-4-fluorophenyl)ethan-1-amine

試薬・触媒・溶媒 2

HCID 517166Dichlorocobalt hexahydrate触媒HCID 887Methanol溶媒

実験手順

Sodium borohydride (1.73 g, 45.51 mmol) was added portionwise to a solution of 2-chloro-4-fluorophenylacetonitrile (1.04 g, 6.15 mmol) and cobalt (II) chloride hexahydrate (2.18 g, 9.22 mmol) in methanol (30 mL) and the mixture was stirred at room temperature for 3 hours. The suspension was then filtered though Celite®, concentrated in vacuo and the residue was partitioned between 1M hydrochloric acid (40 mL) and dichloromethane (40 mL). The aqueous phase was separated, basified to pH 11 with 1M ammonia solution and extracted with dichloromethane (2×40 mL). The combined organic solution was washed with brine (30 mL), dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 98:2:0.2, to afford the title compound as a yellow oil, 350 mg.

後処理

  1. filtrationThe suspension was then filtered though Celite®
  2. concentrationconcentrated in vacuo
  3. customthe residue was partitioned between 1M hydrochloric acid (40 mL) and dichloromethane (40 mL)
  4. customThe aqueous phase was separated
  5. extractionextracted with dichloromethane (2×40 mL)
  6. washThe combined organic solution was washed with brine (30 mL)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by column chromatography on silica gel
  10. washeluting with dichloromethane

出典と根拠

ORDレコード
ord-11d727eb596642eeb93a3363e9fdedd9
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07538141B2

反応ノート

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