2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

Base Information

Chemical Name:2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate
CAS No.:642471-38-3
Molecular Formula:C₄₉H₅₂O₁₂
Molecular Weight:832.945
Hs Code.:

Synonyms:2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

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Chemical Property of 2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

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Technology Process of 2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

There total 8 articles about 2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: 150623-73-7
4-(6-acryloyloxyhexyloxy)cinnamic acid

: 642471-37-2
(R)-2-hydroxy-2-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

: 642471-38-3
2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1080/15421400600700299

Reference yield:

: 83883-26-5
4-{[6-(acryloyloxy)hexyl]oxy}benzoic acid

: 642471-38-3
2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: N,N'-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH₂Cl₂ / 24 h / 20 °C

2: 3.2 g / pyridinium 4-toluenesulfonate / ethanol / 15 h / 60 °C

3: 80 percent / N,N'-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH₂Cl₂ / 24 h / 20 °C

With dmap; pyridinium p-toluenesulfonate; dicyclohexyl-carbodiimide; In ethanol; dichloromethane;
DOI:10.1080/15421400600700299

Reference yield:

: 56772-46-4
ethoxymethyl 4-hydroxybenzoate

: 642471-38-3
2-[4-(6-acryloyloxyhexyloxy)cinnamoyloxy]-2-(R)-phenylethyl 4-[4-(6-acryloyloxyhexyloxy)benzoyloxy]benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: N,N'-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH₂Cl₂ / 24 h / 20 °C

2: 3.2 g / pyridinium 4-toluenesulfonate / ethanol / 15 h / 60 °C

3: 80 percent / N,N'-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH₂Cl₂ / 24 h / 20 °C

With dmap; pyridinium p-toluenesulfonate; dicyclohexyl-carbodiimide; In ethanol; dichloromethane;
DOI:10.1080/15421400600700299