p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

Base Information

Chemical Name:p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside
CAS No.:123826-53-9
Molecular Formula:C₃₇H₃₇ClO₉
Molecular Weight:661.148
Hs Code.:

Synonyms:p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-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 p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

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Technology Process of p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

There total 4 articles about p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-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: 81.0%

: 123826-50-6
p-methoxyphenyl 3,6-di-O-benzyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

: 541-88-8
Chloroacetic anhydride

: 123826-53-9
p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

Guidance literature:: With sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 20 ℃; for 18h;
DOI:10.1016/0008-6215(89)85173-0

Reference yield:

: 874-60-2
4-methyl-benzoyl chloride

: 123826-53-9
p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / pyridine / 4 h / -20 °C

2: 81 percent / NaHCO₃ / dimethylformamide / 18 h / 20 °C

With pyridine; sodium hydrogencarbonate; In N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(89)85173-0

Reference yield:

: 121238-27-5
2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl trichloroimidate

: 123826-53-9
p-methoxyphenyl 3,6-di-O-benzyl-4-O-chloroacetyl-2-O-p-methylbenzoyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / pyridine / 4 h / -20 °C

2: 81 percent / NaHCO₃ / dimethylformamide / 18 h / 20 °C

With pyridine; sodium hydrogencarbonate; In N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(89)85173-0