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Vinyl Acetate → Triethylene glycol monovinyl ether monoacetate

HRID 1792251
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인쇄 미리보기

반응식

HRID 1792251 반응식
[C:1]([O-:4])(=[O:3])[CH3:2].[Na+].C(O)COCCOCCO.C(OC=C)(=O)C.[CH:22]([O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][O:30][CH2:31][CH2:32]OC=C)=[CH2:23].C(OCCOCCOCCO)=C>C1(C)C=CC=CC=1>[C:1]([O:4][CH2:32][CH2:31][O:30][CH2:29][CH2:28][O:27][CH2:26][CH2:25][O:24][CH:22]=[CH2:23])(=[O:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 7904Vinyl AcetateHCID 8172Triethylene GlycolHCID 517045Sodium AcetateHCID 575880Ethanol, 2-(2-(2-(ethenyloxy)ethoxy)ethoxy)-HCID 3033992Triethylene glycol divinyl ether

생성물 1

HCID 22034547Triethylene glycol monovinyl ether monoacetate

시약·촉매·용매 1

HCID 1140
Toluene
용매

반응 조건

온도
100 °C

실험 절차

To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (0.01 mmol) and sodium acetate (1.2 mmol) in toluene (2.0 ml),triethylene glycol (1 mmol) and vinyl acetate (4 mmol) were added, followed by stirring at 100° C. in an atmosphere of argon gas for 6 hours. The reaction mixture was analyzed by gas chromatography to find that triethylene glycol divinyl ether, triethylene glycol monovinyl ether, and triethylene glycol monovinyl ether monoacetate were produced in yields of 63%, 3%, and 18%, respectively, with a conversion from triethylene glycol of 100%.

후처리

  1. additionwere added

출처 및 근거

ORD 기록
ord-23d6d4ffa44348848a0b664c32a65c64
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074970B2

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