Production Method 1

107-21-1

818-61-1

Reaction Conditions

1.1 Reagents: Hydroquinone Catalysts: 1,5-Naphthalenedisulfonic acid Solvents: Benzene ;  5 h, 80 - 85 °C

Reference

Synthesis of (met)acrylic monoesters of ethylene glycol

Mamedov, M. K.; et al, Azerbaidzhanskii Khimicheskii Zhurnal, 2014, (4), 34-37

Production Method 2

818-61-1

Reaction Conditions

1.1 Reagents: Sodium hydroxide Catalysts: Hydroquinone ;  rt → reflux; 4 h, reflux

Reference

Synthesis and characterization of fluorinated polyacrylate graft copolymers capable as water and oil repellent finishing agents

Tang, Weiyi; et al, Journal of Applied Polymer Science, 2011, 119(1), 84-92

Production Method 3

10192-85-5

818-61-1

Reaction Conditions

1.1 Solvents: Acetonitrile

Reference

Synthesis of functionalized acrylates

Curci, Michele; et al, Organic Preparations and Procedures International, 1993, 25(6), 649-57

Production Method 4

5124-30-1

25190-06-1

110-63-4

818-61-1

Reaction Conditions

1.1 Catalysts: Ethyl 4-(dimethylamino)benzoate ,  Camphorquinone ;  3 min

Reference

Design and Preparation of Tertiary Amine Modified Polyurethane Acrylate Oligomer with Co-Initiation/Polymerization Bifunctions for Photo-Curable Inkjet Printing of Textiles

Meng, Yiding; et al, Macromolecular Materials and Engineering, 2020, 305(7),

Production Method 5

818-61-1

2210-25-5

818-61-1

Reaction Conditions

1.1 Reagents: Butylamine ,  Triphenylphosphine Solvents: Tetrahydrofuran ;  2 h, rt

Reference

New insights into the effects of molecular weight and end group on the temperature-induced phase transition of poly(N-isopropylacrylamide) in water

Qiu, Xing Ping; et al, Science China: Chemistry, 2013, 56(1), 56-64

Production Method 6

25322-68-3

814-68-6

818-61-1

Reaction Conditions

1.1 Solvents: Dichloromethane ;  15 min, rt

Reference

Microwave-enhanced liquid-phase synthesis of thiohydantoins and thioxotetrahydropyrimidinones

Yeh, Wen-Ben; et al, Molecular Diversity, 2003, 7(2-4), 185-198

Production Method 7

107-21-1

818-61-1

Reaction Conditions

1.1 Reagents: Iodine ;  4 h, reflux

Reference

New monomers for fullerene-containing polymers

Torosyan, S. A.; et al, Russian Journal of Organic Chemistry, 2014, 50(2), 179-182

Production Method 8

818-61-1

Reaction Conditions

1.1 Reagents: Hydroquinone ,  Sodium hydroxide

Reference

New synthesis of β-hydroxyethyl acrylate

Gao, Dabin, Huaxue Shiji, 1993, 15(4),

Production Method 9

107-21-1

814-68-6

818-61-1

Reaction Conditions

1.1 Reagents: Triethylamine Solvents: Dichloromethane ;  0 °C

Reference

Preparation of biomass-based transparent pressure sensitive adhesives for optically clear adhesive and their adhesion performance

Baek, Seung-Suk; et al, European Polymer Journal, 2017, 92, 97-104

Production Method 10

107-21-1

818-61-1

Reaction Conditions

1.1 Solvents: 2-Methyl-2-butanol ;  120 h, 50 °C

Reference

Hydroxy functional acrylate and methacrylate monomers prepared via lipase-catalyzed transacylation reactions

Popescu, Dragos; et al, Journal of Molecular Catalysis B: Enzymatic, 2009, 62(1), 81-90

Production Method 11

818-61-1

45103-58-0

200128-05-8

818-61-1

Reaction Conditions

1.1 Reagents: Sodium methoxide Solvents: Methanol ,  Acetonitrile ;  overnight, rt

Reference

Versatile thiolated thermosensitive polymers synthesized by ATRP of MEO2MA and AcSEMA, a new methacrylic monomer with a protected thiol group

Liras, Marta; et al, Polymer Chemistry, 2013, 4(24), 5751-5759

2-Hydroxyethyl acrylate Raw materials

• Polyethylene Glycol
• Ethylene Glycol, Dehydrated
• Potassium acrylate
• Dicyclohexylmethane-4,4'-diiso cyanate
• 2-Hydroxyethyl acrylate
• N-Isopropylacrylamide
• 2-(2-Methoxyethoxy)ethyl methacrylate
• terathane(R) 1400
• Acryloyl chloride
• 1,4-Butanediol
• 2-(Acetylthio)-ethyl methacrylate

2-Hydroxyethyl acrylate Preparation Products

• 2-Hydroxyethyl acrylate (818-61-1)

• 1. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
• 2. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
• 3. Enabling high-throughput single-animal gene-expression studies with molecular and micro-scale technologies
  Jason Wan Lab Chip, 2020,20, 4528-4538
• 4. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 5. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
  Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Acrylic acids and derivatives Acrylic acid esters
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

• 102250-59-9(2-Propenoic acid polymer with ethyl 2-propenoate and 2-methoxyethyl 2-propenoate)
• 169381-50-4(2-Propenoic acid, 2-(2-ethoxyethoxy)ethyl ester, polymer with 2-hydroxyethyl 2-propenoate)
• 19812-60-3(2-[2-[2-(2-Hydroxyethoxy)ethoxy]ethoxy]ethyl acrylate)
• 13533-05-6(2-Propenoic acid,2-(2-hydroxyethoxy)ethyl ester)
• 17831-71-9(Tetraethylene Glycol Diacrylate (stabilized with MEHQ))
• 27015-29-8(POLY(2-(2-ETHOXYETHOXY) ETHYL ACRYLATE))
• 26570-48-9(Ethylene glycol diacrylate)
• 106-74-1(2-Ethoxyethyl acrylate)
• 28628-64-0(2-Propenoic acid,2-methoxyethyl ester, homopolymer)
• 16695-45-7(2-Propenoic acid,2-[2-(2-hydroxyethoxy)ethoxy]ethyl ester)