Production Method 1

926-02-3

Reaction Conditions

1.1 Catalysts: Potassium tert-butoxide ,  1,4-Diethoxybutane

Reference

Process and catalysts for the preparation of alkenyl ethers by the addition reaction of alkynes with alcohols

, Germany, , ,

Production Method 2

926-02-3

Reaction Conditions

1.1 Reagents: Potassium

Reference

Chemistry of acetylenic ethers. LII. Acetylenic tert-butyl ethers and other acetylenic ethers with branched alkyl groups. The preparation and pyrolysis of acetylenic ethers

van Daalen, J. J.; Kraak, A.; Arens, J. F., Recueil des Travaux Chimiques des Pays-Bas, 1961, 80, 810-18

Production Method 3

926-02-3

Reaction Conditions

1.1 Catalysts: Triethylamine ,  4,7-Diphenyl-1,10-phenanthroline ,  Palladium trifluoroacetate ;  13 h, 75 °C

Reference

Synthesis of Allyl and Alkyl Vinyl Ethers Using an in Situ Prepared Air-Stable Palladium Catalyst. Efficient Transfer Vinylation of Primary, Secondary, and Tertiary Alcohols

Bosch, Martin; Schlaf, Marcel, Journal of Organic Chemistry, 2003, 68(13), 5225-5227

Production Method 4

637-92-3

926-02-3

Reaction Conditions

1.1 Reagents: 3,3-Dimethyl-1-butene ,  Sodium tert-butoxide Catalysts: [1,8-Bis[bis(1-methylethyl)phosphino-κP]-9,10[1′,2′]-benzenoanthracen-9(10H)-yl-… Solvents: Diethyl ether ;  15 h, 120 °C

Reference

Iridium Pincer-Catalyzed Dehydrogenation of Ethers Featuring Ethylene as the Hydrogen Acceptor

Lyons, Thomas W.; Bezier, David; Brookhart, Maurice, Organometallics, 2015, 34(16), 4058-4062

Production Method 5

926-02-3

Reaction Conditions

Reference

Product subclass 3: enol ethers

Milata, V.; Radl, S.; Voltrova, S., Science of Synthesis, 2008, 32, 589-756

Production Method 6

926-02-3

Reaction Conditions

Reference

Total Synthesis of (+)-Haperforin G

Zhang, Wei; Zhang, Zhenyu; Tang, Jun-Chen; Che, Jin-Teng; Zhang, Hao-Yu; et al, Journal of the American Chemical Society, 2020, 142(46), 19487-19492

Production Method 7

926-02-3

Reaction Conditions

Reference

Application of 1-tert-butoxy-3-[(trimethylsilyl)oxy]buta-1,3-diene in the preparation of functionalized β-hydroxycyclohexanone derivatives, including valuable precursors of daunomycinone analogs

Potman, R. P.; Janssen, N. J. M. L.; Scheeren, J. W.; Nivard, R. J. F., Journal of Organic Chemistry, 1984, 49(19), 3628-34

Production Method 8

926-02-3

Reaction Conditions

1.1 Reagents: Potassium tert-butoxide
1.2 -
1.3 Solvents: Water

Reference

Procedure for the production of tertiary-alkyl alkenyl ethers by the etherification of tertiary alkanols with alkynes in the presence of alkali metal bases

, Germany, , ,

Production Method 9

926-02-3

Reaction Conditions

1.1 Reagents: Potassium hydroxide Catalysts: Lithium diisopropylamide Solvents: 1,3-Dimethyl-2-imidazolidinone ,  Tetrahydrofuran ,  Cyclohexane ;  2 h, rt → 50 °C; 50 °C → reflux; 2 h, reflux; 10 min, 70 °C
1.2 60 - 65 °C

Reference

Process for preparation of tert-butyl vinyl ether

, China, , ,

Production Method 10

7580-85-0

926-02-3

Reaction Conditions

1.1 Catalysts: Silica ,  Cesium oxide ;  1 atm, 380 °C

Reference

New method of production of vinyl ether by vapor phase intramolecular dehydration of glycol ether over solid catalysts

Shimasaki, Yuuji; Ariyoshi, Kimio; Kambe, Hideyuki; Yano, Hitoshi; Ugamura, Shukichi, Journal of Molecular Catalysis A: Chemical, 2006, 256(1-2), 37-42

Production Method 11

926-02-3

2628-17-3

926-02-3

Reaction Conditions

1.1 Catalysts: Pyridinium p-toluenesulfonate Solvents: 1-Methoxy-2-propyl acetate ;  25 °C; 5 h, 20 °C

Reference

Positive photosensitive composition

, European Patent Organization, , ,

Production Method 12

765-14-0

926-02-3

Reaction Conditions

1.1 Reagents: Mercuric acetate

Reference

Highly Isotactic Poly(vinyl alcohol). 2. Preparation and Characterization of Isotactic Poly(vinyl alcohol)

Ohgi, H.; Sato, T., Macromolecules, 1999, 32(8), 2403-2409

Production Method 13

7580-85-0

926-02-3

Reaction Conditions

1.1 Catalysts: Silica ,  Diammonium hydrogen phosphate ,  Cesium nitrate Solvents: Water ;  heated
1.2 380 mm Hg, 450 °C

Reference

Gas-phase intramolecular dehydration process for the manufacture of alkyl vinyl ethers from glycol ethers and distillation processes for product and unreacted starting material recovery

, European Patent Organization, , ,

Production Method 14

926-02-3

Reaction Conditions

Reference

An organic thiyl radical catalyst for enantioselective cyclization

Hashimoto, Takuya; Kawamata, Yu; Maruoka, Keiji, Nature Chemistry, 2014, 6(8), 702-705

Production Method 15

926-02-3

Reaction Conditions

Reference

17O NMR spectra of vinyl ethers

Taskinen, Esko; Hellman, Jaakko, Magnetic Resonance in Chemistry, 1994, 32(6), 353-7

Production Method 16

926-02-3

Reaction Conditions

Reference

Preparation of vinyl ethers by transetherification in the presence of molecular sieves

Yuki, Heimei; Hatada, Koichi; Nagata, Kazuhiko; Kajiyama, Kenichi, Bulletin of the Chemical Society of Japan, 1969, 42(12), 3546-50

tert-Butyl vinyl ether - Raw materials

• tert-Butyl vinyl ether -
• 4-Vinylphenol
• Dodecyl vinyl ether
• Ethylene glycol mono-tert-buthyl ether
• tert-Butyl Ethyl Ether

tert-Butyl vinyl ether - Preparation Products

• tert-Butyl vinyl ether - (926-02-3)

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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Organooxygen compounds
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds

• 4188-70-9(2-tert-Butoxyprop-1-ene)
• 52752-57-5(1-tert-Butoxybuta-1,3-diene)
• 52752-58-6(1,3-BUTADIENE, 1-(1,1-DIMETHYLETHOXY)-, (1E)-)
• 89599-49-5(Propane, 2-[(2-bromoethenyl)oxy]-2-methyl-)
• 926-65-8(Isopropyl vinylether)
• 29281-39-8(Butane,2-(ethenyloxy)-2-methyl-)
• 4188-71-0(1-Propene,1-(1,1-dimethylethoxy)-, (1Z)-)
• 113279-39-3((Z)-1-Bromo-2-tert-butoxyethene)
• 78968-65-7(Propane, 2,2'-[(1Z)-1,2-ethenediylbis(oxy)]bis[2-methyl-)
• 86528-15-6(1,4-Di-tert-butoxybuta-1,3-diene)