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Ammonium Hydroxide → 4,4-Difluorocyclohexanecarboxamide

HRID 1049324
ノート
印刷プレビュー

反応式

HRID 1049324 の反応式
[F:1][C:2]1([F:11])[CH2:7][CH2:6][CH:5]([C:8](O)=[O:9])[CH2:4][CH2:3]1.C(Cl)(=O)C(Cl)=O.[NH4+:18].[OH-]>C(Cl)Cl.CN(C=O)C.C1COCC1.[Cl-].[Na+].O>[F:1][C:2]1([F:11])[CH2:7][CH2:6][CH:5]([C:8]([NH2:18])=[O:9])[CH2:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 14923Ammonium HydroxideHCID 65578Oxalyl chlorideHCID 27791364,4-Difluorocyclohexanecarboxylic acid

生成物 1

HCID 469422314,4-Difluorocyclohexanecarboxamide収率 77.4%

試薬・触媒・溶媒 4

HCID 6228Dimethylformamide触媒HCID 6344Dichloromethane溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 57417360Sodium chloride; water溶媒

実験手順

A solution of 4,4-difluorocyclohexanecarboxylic acid (0.217 g, 1.322 mmol) in DCM (4 mL) was treated with oxalyl chloride (0.174 mL, 1.983 mmol) followed by catalytic DMF (1 drop) and the mixture stirred at RT for 1.5 h. The mixture was concentrated to dryness, co-evaporated with DCM (1×) and the resulting residue dissolved in THF (2 mL), added to a stirring solution of NH4OH (˜14M, 2 mL, 28.0 mmol) in THF (2 mL) and stirred for 30 minutes. The mixture was diluted with brine, extracted with EtOAc (3×) and the combined organics were dried over MgSO4 and concentrated to dryness to afford 4,4-difluorocyclohexanecarboxamide (167 mg, 77%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 7.28 (s, 1H), 6.79 (s, 1H), 2.20 (m, 1H), 2.00 (m, 2H), 1.86-1.67 (m, 4H), 1.57 (m, 2H).

後処理

  1. concentrationThe mixture was concentrated to dryness, co-evaporated with DCM (1×)
  2. dissolutionthe resulting residue dissolved in THF (2 mL)
  3. stirringstirred for 30 minutes
  4. extractionextracted with EtOAc (3×)
  5. dry with materialthe combined organics were dried over MgSO4
  6. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-e481285497f24033a19702b19b09a06e
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09382228B2

反応ノート

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