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Hydrochloric Acid → 2-(1Adamantyl)-n-pentylethylamine hydrochloride

HRID 11432
ノート
印刷プレビュー

反応式

HRID 11432 の反応式
[CH2:1]([NH2:6])[CH2:2][CH2:3][CH2:4][CH3:5].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].CS(O[CH2:20][CH2:21][C:22]12[CH2:31][CH:26]3[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]3)[CH2:23]1)[CH2:29]2)(=O)=O.[ClH:32]>C(O)C.C(OCC)(=O)C>[ClH:32].[C:22]12([CH2:21][CH2:20][NH:6][CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[CH2:31][CH:26]3[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]3)[CH2:23]1)[CH2:29]2
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 5

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 8060PentylamineHCID 11430Potassium CarbonateHCID 157176822-(1-Adamantyl)ethyl methanesulfonate

生成物 1

HCID 498316802-(1Adamantyl)-n-pentylethylamine hydrochloride

試薬・触媒・溶媒 2

HCID 702
Ethanol
溶媒
HCID 8857Ethyl Acetate溶媒2 回

実験手順

Pentylamine (2.69 ml, 23.2 mmol), potassium carbonate (2.14 g, 15.5 mmol) and sodium iodide (2.30 g, 15.3 mmol) were added to a solution of 2-(1-adamantyl)ethyl methanesulfonate (2.07 g, 8.01 mmol) in ethanol (45.8 ml), and the mixture was refluxed for 17 hours. The reaction mixture was concentrated under reduced pressure, and the concentrate was diluted with chloroform (100 ml). This was washed with a 1 N aqueous sodium hydroxide solution (100 ml) and a saturated aqueous sodium chloride solution (100 ml) successively, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography. A 4 N solution of hydrogen chloride in ethyl acetate (3.1 ml) was added to a solution of the resulting free form (1.52 g, 6.10 mmol) of the titled compound in ethyl acetate (0.50 ml). The precipitated solid was washed with ethyl acetate and filtered off to give 1.33 g (60%) of the titled compound.

後処理

  1. temperaturethe mixture was refluxed for 17 hours
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additionthe concentrate was diluted with chloroform (100 ml)
  4. washThis was washed with a 1 N aqueous sodium hydroxide solution (100 ml)
  5. dry with materiala saturated aqueous sodium chloride solution (100 ml) successively, and the organic layer was dried over magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-0be30f756b24468c9c36d5c24ba0fe57
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07098226B2

反応ノート

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