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1-Butanol → Acetoxybutoxybutene

HRID 1295425
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인쇄 미리보기

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HRID 1295425 반응식
P([O-])([O-])[O-].[C:5]([O:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][O:13][C:14](=[O:16])[CH3:15])(=O)[CH3:6].[CH2:17](O)[CH2:18]CC.C(OC(OCCCC)=CCC)CCC>[Pd]>[C:14]([O:13][CH2:12][CH2:11][CH2:10][CH2:9][O:8][CH:5]=[CH:6][CH2:17][CH3:18])(=[O:16])[CH3:15]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 2631-ButanolHCID 107908PhosphiteHCID 643799(2Z)-but-2-ene-1,4-diyl diacetate2회HCID 21932110Dibutoxybutene

생성물 1

HCID 86593756Acetoxybutoxybutene수율 25.7%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

The reaction was carried out by adding 0.0020 g (0.0040 mmol) of trisdibenzylideneacetone dipalladium having a palladium content of 21.5 wt % and 0.0173 g (0.0162 mmol) of the above (L-26) bidentate phosphite in an amount of 4 equivalents to a container substituted with nitrogen, adding 1.418 g (8.233 mmol) of cis-1,4-diacetoxy-2-butene and 2.327 g (31.395 mmol) of 1-butanol thereto under nitrogen atmosphere, and heating the resultant mixture at 100° C. After reacting 5 hours, the resultant solution composition was analyzed by gas chromatography, and it was found that cis-1,4-diacetoxy-2-butene was converted at a conversion rate of 97.5%, and 71.8% of dibutoxybutene and 25.7% of acetoxybutoxybutene were produced.

출처 및 근거

ORD 기록
ord-59296aa105794eba9419fcf35a1fe051
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241857B2

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