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

HRID 1384456
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HRID 1384456 반응식
[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]
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참가 물질

4

반응물 2

HCID 76752-(2-Hydroxyethyl)pyridineHCID 178418361HCID 178418361, 화합물2회

생성물 1

HCID 151442-Piperidin-2-ylethanol

시약·촉매·용매 1

HCID 178527103HCID 178527103, 화합물촉매

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-51ab6c36b2c74bfc85d88df13e661cea
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06258955B1

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