Production Method 1

623-47-2

155934-40-0

36997-05-4

82290-07-1

262293-82-3

Reaction Conditions

1.1 Catalysts: Silver triflate ,  2249872-40-8 Solvents: Methanol ;  1 h, 40 °C

Reference

Hydroalkoxylation of terminal and internal alkynes catalyzed by dinuclear gold(I) complexes with bridging Di(N-heterocyclic carbene) ligands

Marcheggiani, Elena; et al, Catalysts, 2020, 10(1),

Production Method 2

623-47-2

155934-40-0

82290-07-1

Reaction Conditions

1.1 Catalysts: Platinum dichloride ;  48 h, rt

Reference

Platinum- and gold-catalyzed hydroalkoxylation and tetramerization of propiolate esters

Chen, Qian; et al, Catalysis Communications, 2014, 56, 101-105

Production Method 3

623-47-2

155934-40-0

82290-07-1

262293-82-3

Reaction Conditions

1.1 Catalysts: Platinum dichloride ;  12 h, rt

Reference

Platinum- and gold-catalyzed hydroalkoxylation and tetramerization of propiolate esters

Chen, Qian; et al, Catalysis Communications, 2014, 56, 101-105

2-Propenoic acid, 3-methoxy-, ethyl ester, (2Z)- Raw materials

• ethyl propiolate

2-Propenoic acid, 3-methoxy-, ethyl ester, (2Z)- Preparation Products

• 2-Propenoic acid, 3-methoxy-, ethyl ester, (2Z)- (155934-40-0)
• 2-Propenoic acid,2-methoxy-, ethyl ester (36997-05-4)
• 3-Methoxypropenoic acid ethyl ester (82290-07-1)
• ETHYL 3,3-DIMETHOXYPROPANOATE (262293-82-3)

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• 4. Acentric and chiral heterometallic inorganic–organic hybrid frameworks mediated by alkali or alkaline earth ions: synthesis and NLO properties
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  Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471

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