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Hydrochloric Acid → 2-Phenyl-2-(pyrrolidin-1-yl)acetic acid hydrochloride

HRID 404630
ノート
印刷プレビュー

反応式

HRID 404630 の反応式
[C:1]1([CH:7]([N:13]2[CH2:17][CH2:16][CH2:15][CH2:14]2)[C:8]([O:10]CC)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:18]>O1CCOCC1>[ClH:18].[C:1]1([CH:7]([N:13]2[CH2:17][CH2:16][CH2:15][CH2:14]2)[C:8]([OH:10])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 313Hydrochloric Acid2 回HCID 3568733Ethyl 2-phenyl-2-(pyrrolidin-1-yl)acetate

生成物 1

HCID 66031122-Phenyl-2-(pyrrolidin-1-yl)acetic acid hydrochloride収率 79%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

Ethyl 2-phenyl-2-(pyrrolidin-1-yl)acetate (0.31 g, 1.33 mmol) was dissolved in dioxane (11 ml) and 37% HCl (1.09 ml, 13.3 mmol) was added dropwise. The mixture was stirred at reflux overnight. Then 37% HCl (1.09 ml, 13.3 mmol) was added again and the reaction was refluxed for additional 24 hours. The solvent was evaporated, the residue was triturated with acetonitrile (10 ml) and the suspension was filtered on a buckner funnel. The solid was recovered to obtain 2-phenyl-2-(pyrrolidin-1-yl)acetic acid hydrochloride (0.25 g, 79% yield) as a white solid.

後処理

  1. temperatureat reflux overnight
  2. temperaturethe reaction was refluxed for additional 24 hours
  3. customThe solvent was evaporated
  4. customthe residue was triturated with acetonitrile (10 ml)
  5. filtrationthe suspension was filtered on a buckner funnel
  6. customThe solid was recovered

出典と根拠

ORDレコード
ord-b6a6c74acd004fe280572b857281e079
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08748613B2

反応ノート

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