3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

Base Information

Chemical Name:3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside
CAS No.:1271934-22-5
Molecular Formula:C₂₃H₂₆O₄
Molecular Weight:366.457
Hs Code.:

Synonyms:3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

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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 3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

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Technology Process of 3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

There total 2 articles about 3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside 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: 93.0%

: 1271934-18-9
3-(2-phenyl-benzo[b]furan-3-yl)-propyl 4-O-acetyl-2,3,6-trideoxy-α-L-erythro-hexopyranoside

: 1271934-22-5
3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

Guidance literature:: With methanol; potassium carbonate; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2011.01.014

Reference yield:

: 1192235-32-7
3-(2-phenyl-benzo[b]furan-3-yl)-prop-2-ynyl 4-O-acetyl-2,3,6-trideoxy-α-L-erythro-hexopyranoside

: 1271934-22-5
3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 °C / 760.05 Torr

2: methanol; potassium carbonate / 12 h / 20 °C

With methanol; palladium 10% on activated carbon; hydrogen; potassium carbonate; In ethyl acetate;
DOI:10.1016/j.bmc.2011.01.014

Reference yield:

: 1271934-22-5
3-(2-phenyl-benzo[b]furan-3-yl)-propyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

: 1271934-14-5
3-(2-phenyl-benzo[b]furan-3-yl)-propyl 4-amino-2,3,4,6-tetradeoxy-α-L-threo-hexopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: di-isopropyl azodicarboxylate; diphenyl phosphoryl azide; triphenylphosphine / tetrahydrofuran / 12 h / -20 - 20 °C

2: water; triphenylphosphine / tetrahydrofuran / 10 h / Reflux

With di-isopropyl azodicarboxylate; diphenyl phosphoryl azide; water; triphenylphosphine; In tetrahydrofuran; 1: Mitsunobu reaction / 2: Staudinger reaction;
DOI:10.1016/j.bmc.2011.01.014