p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

Base Information

Chemical Name:p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside
CAS No.:253603-12-2
Molecular Formula:C₄₂H₅₁N₂O₁₀P
Molecular Weight:774.848
Hs Code.:

Synonyms:p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

Suppliers and Price of p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

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Technology Process of p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

There total 5 articles about p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside 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: 92.0%

: p-aminophenyl 2,3,4-tri-O-benzyl-6-O-phosphocholine-α-D-glucopyranoside

: 920-46-7,26937-45-1
Methacryloyl chloride

: 253603-12-2
p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

Guidance literature:: With triethylamine; In dichloromethane; for 1h;
DOI:10.1080/07328309908544048

Reference yield:

: 55357-38-5
choline tosylate

: 253603-12-2
p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 53 percent

2: 92 percent / hydrogen / Pd(OH)2/C / methanol / 7 h / 20 °C

3: 92 percent / triethylamine / CH₂Cl₂ / 1 h

With hydrogen; triethylamine; palladium dihydroxide; In methanol; dichloromethane; 2: Catalytic hydrogenation / 3: Acylation;
DOI:10.1080/07328309908544048

Reference yield:

: 221697-42-3
p-nitrophenyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside

: 253603-12-2
p-methacryloylamidophenyl 2,3,4-tri-O-benzyl-6-O-phosphorylcholine-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 53 percent

2: 92 percent / hydrogen / Pd(OH)2/C / methanol / 7 h / 20 °C

3: 92 percent / triethylamine / CH₂Cl₂ / 1 h

With hydrogen; triethylamine; palladium dihydroxide; In methanol; dichloromethane; 2: Catalytic hydrogenation / 3: Acylation;
DOI:10.1080/07328309908544048