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2-Methyl-2-butanol → 1-[(1-Butoxyethenyl)oxy]butane

HRID 2209854
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HRID 2209854 반응식
Cl[CH2:2][CH:3]([O:9][CH2:10][CH2:11][CH2:12][CH3:13])[O:4][CH2:5][CH2:6][CH2:7][CH3:8].CC(O)(CC)C.[OH-].[K+]>COC(C)(C)C>[CH2:10]([O:9][C:3]([O:4][CH2:5][CH2:6][CH2:7][CH3:8])=[CH2:2])[CH2:11][CH2:12][CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 64052-Methyl-2-butanolHCID 14797Potassium HydroxideHCID 134066061-(1-Butoxy-2-chloroethoxy)butane

생성물 1

HCID 130466131-[(1-Butoxyethenyl)oxy]butane

시약·촉매·용매 1

HCID 15413tert-Butyl methyl ether용매

실험 절차

209 g (1 mol) of 1-chloro-2,2-dibutoxyethane, 300 ml of tert.-butyl methyl ether, 13.2 g (0.13 mol) of 2-methyl-2-butanol, 8 g of polyethylene glycol 1000 dimethyl ether and 200 g (3 mol) of technical grade potassium hydroxide were heated under reflux while stirring for six hours. The reaction mixture was worked up as described above. The conversion was 77.1% of theoretical, the yield of pure material was 60.8% of theoretical (b.p. 87°-88° C., 1.5 kPa).

후처리

  1. temperatureunder reflux

출처 및 근거

ORD 기록
ord-b99fe51ed09045c1b360ea208081bde4
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05455361

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