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Octanal → 2-Methylene-octanal

HRID 15622
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인쇄 미리보기

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HRID 15622 반응식
[CH:1](=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C=O.[CH2:12](NCCCC)CCC.C(O)(=O)CCCCCCCCC>>[CH2:12]=[C:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH:1]=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 454Octanal2회HCID 712FormaldehydeHCID 2969Decanoic AcidHCID 8148Dibutylamine

생성물 1

HCID 112057952-Methylene-octanal수율 1,636.4%

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온도
95 °C

실험 절차

A 2 L four-necked flask equipped with a stirrer, a thermometer and a reflux condenser was charged with 762 g (6.0 mol) of n-octanal, 520 g (6.4 mol) of a 37% by mass formaldehyde aqueous solution, 15 g (0.33 mol) of dibutyl amine and 10 g (0.06 mol) of decanoic acid, and the contents in the flask were stirred while heating at 95° C. After the elapse of 45 min, it was confirmed that no n-octanal was present in the raw mixture, and then the mixture was cooled and separated into two layers. The thus separated organic layer was subjected to distillation treatment, thereby obtaining 790 g (5.4 mol) of a-methylene octanal (purity as measured by gas chromatography: 95%) (yield based on theoretical amount: 90%).

후처리

  1. customA 2 L four-necked flask equipped with a stirrer
  2. customAfter the elapse of 45 min, it
  3. temperaturethe mixture was cooled
  4. customseparated into two layers
  5. distillationThe thus separated organic layer was subjected to distillation treatment

출처 및 근거

ORD 기록
ord-4587e73c346047e7ae98bdbb2f4f0c05
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732644B2

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