1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

Base Information

Chemical Name:1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol
CAS No.:116454-02-5
Molecular Formula:C₃₃H₃₂O₄S
Molecular Weight:524.681
Hs Code.:

Synonyms:1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

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Chemical Property of 1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

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Technology Process of 1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

There total 6 articles about 1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol 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: 70.0%

: 141810-66-4
phenyl 3,4,6-tri-O-benzyl-2-O-phenoxythiocarbonyl-1-thio-α-D-mannopyranoside

: 116454-02-5
1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

Guidance literature:: With N-iodo-succinimide; molecular sieve; trifluorormethanesulfonic acid; In diethyl ether; 1,2-dichloro-ethane; for 0.0833333h;
DOI:10.1016/S0040-4020(01)80165-4

Reference yield: 70.0%

: 55628-54-1
3,4,6-tri-O-benzyl-D-glucal

: 931-59-9
benzenesulfenyl chloride

: 116454-02-5
1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene;
DOI:10.1016/S0040-4039(00)99257-8

Reference yield:

: 138181-67-6,127299-78-9
phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside

: 116454-02-5
1,5-Anhydro-3,4,6-tri-O-benzyl-1,2-didesoxy-2-phenylthio-D-arabino-hex-1-enitol

Guidance literature:: Multi-step reaction with 3 steps

1: sodium methoxide / methanol / 2 h / Ambient temperature

2: DMAP / acetonitrile / 16 h / Ambient temperature

3: 70 percent / N-iodosuccinimide, trifluoromethanesulfonic acid, molecular sieves / 1,2-dichloro-ethane; diethyl ether / 0.08 h

With dmap; N-iodo-succinimide; molecular sieve; trifluorormethanesulfonic acid; sodium methylate; In methanol; diethyl ether; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1016/S0040-4020(01)80165-4