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Phosphoric Acid → 2-[(2,6-Dichloro-3-methylphenyl)amino]phenylmethanol

HRID 343884
ノート
印刷プレビュー

反応式

HRID 343884 の反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:19])=[C:6]([NH:9][C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:15]=2[C:16](O)=[O:17])[C:7]=1[Cl:8].[H-].[H-].[H-].[H-].[Li+].[Al+3].OP(O)(O)=O>C1COCC1>[Cl:8][C:7]1[C:2]([CH3:1])=[CH:3][CH:4]=[C:5]([Cl:19])[C:6]=1[NH:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:15]=1[CH2:16][OH:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1004Phosphoric AcidHCID 4037Meclofenamic AcidHCID 21226445Aluminium lithium hydride

生成物 1

HCID 150273752-[(2,6-Dichloro-3-methylphenyl)amino]phenylmethanol収率 56%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred solution of meclofenamic acid (4.27 g, 13.4 mmol) in THF (75 mL) at 0° C. was added LiAlH4 (1.02 g, 26.8 mmol) in portions over 0.5 hour. The mixture was maintained cold for 2 hrs after which it was slowly added to a cold solution of H3PO4 (1M, 100 mL) and extracted with ethyl ether (3×75 mL). The combined organic layers were washed with water and brine, dried over MgSO4. filtered, and evaporated in vacuo. Purification by chromatography on silica gel (9:1 hexanes/ethyl acetate) afforded 2.1 g (56%) of 2-[(2,6-dichloro-3-methylphenyl)amino]phenylmethanol as an off white solid.

後処理

  1. temperatureThe mixture was maintained cold for 2 hrs after which it
  2. extractionextracted with ethyl ether (3×75 mL)
  3. washThe combined organic layers were washed with water and brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customPurification by chromatography on silica gel (9:1 hexanes/ethyl acetate)

出典と根拠

ORDレコード
ord-9a22b0c6c5dd4df999a827f7e6de4f5c
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05863946

反応ノート

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