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2-(2-Hydroxyethyl)pyridine → 2-Piperidin-2-ylethanol

HRID 1384456
ノート
印刷プレビュー

反応式

HRID 1384456 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][CH2:8][OH:9].[H][H]>[Ru]=O>[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[CH2:7][CH2:8][OH:9]
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 76752-(2-Hydroxyethyl)pyridineHCID 178418361HCID 178418361、化合物2 回

生成物 1

HCID 151442-Piperidin-2-ylethanol

試薬・触媒・溶媒 1

HCID 178527103HCID 178527103、化合物触媒

実験手順

Hydrogenations were carried out by charging solvent, when utilized, 246 g of 2-pyridineethanol, and 2.5 g of ruthenium oxide (RuO2) into a pressure vessel capable of agitation, agitating the resulting mixture and pressurizing the vessel and its contents to 500 psig or 1000 psig with hydrogen. Under constant hydrogen pressure and continued agitation, the reaction mixture was heated to the reaction temperature until hydrogen uptake ceased. The pressure vessel and its contents were cooled, vented and the catalyst removed with vacuum filtration. Upon distillation of the filtrate, 2-piperidineethanol was obtained and analyzed on two separate gc columns (6′ CW 20M 160° C. and 15M DB-1 80° C.→220° C.@ 16° C./m capillary column) to provide product yield and composition of the distillate. The results are provided in Table IV. Hydrogenations were also carried out with recycled RuO2 catalyst under the conditions described above. The results of these reactions utilizing recycled catalyst are provided in Table V.

後処理

  1. temperatureThe pressure vessel and its contents were cooled
  2. customthe catalyst removed with vacuum filtration
  3. distillationUpon distillation of the filtrate

出典と根拠

ORDレコード
ord-51ab6c36b2c74bfc85d88df13e661cea
出典データセット
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06258955B1

反応ノート

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