[(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

Base Information

Chemical Name:[(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester
CAS No.:111397-10-5
Molecular Formula:C₃₀H₄₄INO₄Si
Molecular Weight:637.674
Hs Code.:

Synonyms:[(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

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Chemical Property of [(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

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Technology Process of [(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

There total 4 articles about [(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester 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:

: 111397-09-2
[(1R,2S)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-hydroxy-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

: 111397-10-5
[(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

Guidance literature:: With trifluoromethylsulfonic anhydride; sodium iodide; In pyridine;
DOI:10.1039/c39870000166

Reference yield:

: 1611-61-6
3-Methylbut-2-enyl Isocyanate

: 111397-10-5
[(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NaH, NaOH / 2.) tetrahydrofuran

2: NaI, (CF₃SO₂)2O / pyridine

With sodium hydroxide; trifluoromethylsulfonic anhydride; sodium hydride; sodium iodide; In pyridine;
DOI:10.1039/c39870000166

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 111397-10-5
[(1R,2R)-4-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-iodo-butyl]-(3-methyl-but-2-enyl)-carbamic acid phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NaH, NaOH / 2.) tetrahydrofuran

2: NaI, (CF₃SO₂)2O / pyridine

With sodium hydroxide; trifluoromethylsulfonic anhydride; sodium hydride; sodium iodide; In pyridine;
DOI:10.1039/c39870000166