p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

Base Information

Chemical Name:p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside
CAS No.:359687-00-6
Molecular Formula:C₂₉H₄₀O₁₂
Molecular Weight:580.629
Hs Code.:

Synonyms:p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

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Chemical Property of p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

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Technology Process of p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

There total 8 articles about p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 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: 95.0%

: 359686-64-9
p-[2-(benzyloxycarbonyl)ethyl]phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

: 359687-00-6
p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

Guidance literature:: With hydrogen; palladium dihydroxide; In ethanol; for 2h;
DOI:10.1081/CAR-100103953

Reference yield:

: 31770-76-0
3-(4-hydroxyphenyl)propionic acid benzyl ester

: 359687-00-6
p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1.1: 59 percent / SnCl₄ / CH₂Cl₂ / 1 h / -19 °C

2.1: 74 percent / NaOBn / phenylmethanol / 1 h / 0 °C / pH 11

3.1: (Bu₃Sn)2O / toluene / 2 h / Heating

3.2: 66 percent / toluene / 72 h / 20 °C

4.1: 145 mg / pyridine / 4 h / 20 °C

5.1: 87 percent / 18-crown-6 / benzene / 12 h / ultrasonication

6.1: 95 percent / H₂ / Pd(OH)2 / ethanol / 2 h

With pyridine; 18-crown-6 ether; hydrogen; tin(IV) chloride; sodium phenyl-methanolate; bis(tri-n-butyltin)oxide; palladium dihydroxide; In ethanol; dichloromethane; toluene; benzyl alcohol; benzene;
DOI:10.1081/CAR-100103953

Reference yield:

: 501-97-3
4-hydroxyphenylpropionic acid

: 359687-00-6
p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1.1: 765 mg / KHCO₃ / dimethylformamide / 12 h / 20 °C

2.1: 59 percent / SnCl₄ / CH₂Cl₂ / 1 h / -19 °C

3.1: 74 percent / NaOBn / phenylmethanol / 1 h / 0 °C / pH 11

4.1: (Bu₃Sn)2O / toluene / 2 h / Heating

4.2: 66 percent / toluene / 72 h / 20 °C

5.1: 145 mg / pyridine / 4 h / 20 °C

6.1: 87 percent / 18-crown-6 / benzene / 12 h / ultrasonication

7.1: 95 percent / H₂ / Pd(OH)2 / ethanol / 2 h

With pyridine; 18-crown-6 ether; hydrogen; tin(IV) chloride; potassium hydrogencarbonate; sodium phenyl-methanolate; bis(tri-n-butyltin)oxide; palladium dihydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; benzyl alcohol; benzene;
DOI:10.1081/CAR-100103953