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Tetraethylammonium Hydroxide → Ethylene terephthalate, cyclic-(1:1)-

HRID 1085621
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인쇄 미리보기

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HRID 1085621 반응식
[C:1]([OH:12])(=[O:11])[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[Ge](=O)=O.[OH-].[CH2:17]([N+](CC)(CC)CC)[CH3:18]>C(O)CO>[C:1]1(=[O:12])[O:11][CH2:18][CH2:17][O:8][C:6](=[O:7])[C:5]2[CH:9]=[CH:10][C:2]1=[CH:3][CH:4]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6509Tetraethylammonium HydroxideHCID 7489Terephthalic AcidHCID 14796Dioxogermane

생성물 1

HCID 15066111Ethylene terephthalate, cyclic-(1:1)-

시약·촉매·용매 1

HCID 174Ethylene Glycol용매

실험 절차

A mixture of 1734 parts by weight of terephthalic acid and 713 parts by weight of ethylene glycol was stirred for 4 hours under 2 atmospheres. Thereafter, 0.3 part by weight of germanium dioxide, 0.3 part by weight of tetraethylammonium hydroxide and 0.4 part by weight of methyl acid phosphate were added, and the reaction was carried out at 260° C. for 2 hours under 1 atmosphere. The reaction product was withdrawn, cooled, pulverized and dried to obtain 1500 parts by weight of an ethylene terephthalate oligomer.

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후처리

  1. waitthe reaction was carried out at 260° C. for 2 hours under 1 atmosphere
  2. customThe reaction product was withdrawn
  3. temperaturecooled
  4. customdried

출처 및 근거

ORD 기록
ord-084c511c46a44915b66cbc81547ce345
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05010146

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