methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

Base Information

Chemical Name:methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside
CAS No.:808741-16-4
Molecular Formula:C₅₁H₆₄O₁₃
Molecular Weight:885.061
Hs Code.:

Synonyms:methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

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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 methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

There total 7 articles about methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-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: 88.0%

: 3282-30-2
pivaloyl chloride

: 808741-15-3
methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

: 808741-16-4
methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 4h;
DOI:10.1021/ja047194t

Reference yield:

: 3282-30-2
pivaloyl chloride

: 808741-16-4
methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: 98 percent / DMAP; Et₃N / CH₂Cl₂ / 4 h / 20 °C

2.1: 1-(phenylsulfonyl)piperidine; 2,4,6-tri-tert-butylpyrimidine; molecular sieves 3A / CH₂Cl₂ / 0.5 h / -60 °C

2.2: 80 percent / trifluoromethanesulfonic anhydride / CH₂Cl₂ / 6 h / -78 °C

3.1: 85 percent / camphorsulfonic acid; neopentyl glycol / CH₂Cl₂ / 16 h / 20 °C

4.1: 88 percent / DMAP; Et₃N / CH₂Cl₂ / 4 h / 20 °C

With dmap; 1-(phenylsulfonyl)piperidine; 3 A molecular sieve; camphor-10-sulfonic acid; triethylamine; 2,2-Dimethyl-1,3-propanediol; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane;
DOI:10.1021/ja047194t

Reference yield:

: 154125-79-8
methyl β-xylopyranosyl-(1→4)-β-D-mannopyranoside

: 808741-16-4
methyl 2,3-di-O-benzyl-6-O-pivaloyl-4-O-(2,3-di-O-benzyl-6-O-pivaloyl-β-D-mannopyranosyl)-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1.1: 89 percent / camphorsulfonic acid; neopentyl glycol / CH₂Cl₂ / 12 h / 20 °C

2.1: 98 percent / DMAP; Et₃N / CH₂Cl₂ / 4 h / 20 °C

3.1: 1-(phenylsulfonyl)piperidine; 2,4,6-tri-tert-butylpyrimidine; molecular sieves 3A / CH₂Cl₂ / 0.5 h / -60 °C

3.2: 80 percent / trifluoromethanesulfonic anhydride / CH₂Cl₂ / 6 h / -78 °C

4.1: 85 percent / camphorsulfonic acid; neopentyl glycol / CH₂Cl₂ / 16 h / 20 °C

5.1: 88 percent / DMAP; Et₃N / CH₂Cl₂ / 4 h / 20 °C

With dmap; 1-(phenylsulfonyl)piperidine; 3 A molecular sieve; camphor-10-sulfonic acid; triethylamine; 2,2-Dimethyl-1,3-propanediol; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane;
DOI:10.1021/ja047194t