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Acetic Acid → HCID 23344265, 화합물

HRID 27221
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HRID 27221 반응식
[CH3:1][C:2]1([CH3:13])[CH2:7][C:6]([OH:10])([C:8]#[N:9])[CH2:5][C:4]([CH3:12])([CH3:11])[NH:3]1.S(=O)(=O)(O)O.[C:19](O)(=O)[CH3:20]>>[CH2:19]([CH:20]1[NH:9][CH2:8][C:6]2([CH2:5][C:4]([CH3:12])([CH3:11])[NH:3][C:2]([CH3:13])([CH3:1])[CH2:7]2)[O:10]1)[CH2:2][CH2:7][CH2:6][CH2:5][CH:4]([CH3:12])[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 1118Sulfuric Acid2회HCID 908744-Piperidinecarbonitrile, 4-hydroxy-2,2,6,6-tetramethyl-

생성물 1

HCID 23344265HCID 23344265, 화합물

실험 절차

182 g of 2,2,6,6-tetramethyl-4-hydroxy-4-cyanopiperidine, 284 g of isononyl-aldehyde and 200 g of concentrated sulfuric acid are stirred for 25 hours at 60° C. in 600 g of glacial acetic acid in a 2 liter apparatus with agitator. After cooling the main portion of the solvent is distilled off under reduced pressure. The residue is stirred with 500 ml of acetone and suction-filtered, thus yielding 292 g=69% of th. of the sulfuric acid salt of the intended compound.

후처리

  1. temperatureAfter cooling the main portion of the solvent
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • distillationis distilled off under reduced pressure
  • filtrationsuction-filtered
  • customthus yielding 292 g=69% of th
  • 출처 및 근거

    ORD 기록
    ord-c2fadbb5f2ca4eb892744daef57bea8d
    출처 데이터셋
    uspto-grants-1980_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04220773

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