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Hydrochloric Acid → 4-chloro-N1-(tetrahydro-pyran-4-ylmethyl)-benzene-1,2-diamine

HRID 469723
ノート
印刷プレビュー

反応式

HRID 469723 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH2:9][CH:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)=[C:4]([N+:16]([O-])=O)[CH:3]=1.[Sn].Cl.[OH-].[Na+]>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([NH2:16])[C:5]([NH:8][CH2:9][CH:10]2[CH2:11][CH2:12][O:13][CH2:14][CH2:15]2)=[CH:6][CH:7]=1
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 14798Sodium HydroxideHCID 5352426Tin atomHCID 62349965(4-Chloro-2-nitro-phenyl)-(tetrahydro-pyran-4-ylmethyl)-amine

生成物 1

HCID 637259554-chloro-N1-(tetrahydro-pyran-4-ylmethyl)-benzene-1,2-diamine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒

実験手順

To a solution of (4-chloro-2-nitro-phenyl)-(tetrahydro-pyran-4-ylmethyl)-amine (1.28 g; 4.729 mmol) in tetrahydrofuran (25 mL) was added tin metal (1.740 g; 14.660 mmol) and 1N hydrochloric acid (32.157 mL; 32.157 mmol) and the reaction is stirred at room temperature overnight. After this time, the mixture is diluted with 1N sodium hydroxide solution (1.6 g NaOH/40 mL water; 40 mmol) and filtered through Celite®, washing with ethyl acetate. The filtrate is extracted with ethyl acetate and the combined organics are washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo to afford title compound which was used without further purification. ESI m/z 241 [M+H]+

後処理

  1. filtrationfiltered through Celite®
  2. washwashing with ethyl acetate
  3. extractionThe filtrate is extracted with ethyl acetate
  4. washthe combined organics are washed with water and brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-23bacb4b87f04c2bbb88e98ec79c030c
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08629157B2

反応ノート

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