[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester
CAS No.:212330-32-0
Molecular Formula:C₁₇H₂₄N₂O₄
Molecular Weight:320.389
Hs Code.:

Synonyms:[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

Suppliers and Price of [(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of [(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of [(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

There total 2 articles about [(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl 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: 70.0%

: 212330-31-9
[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-(tert-butyl-diphenyl-silanyloxymethyl)-4-trimethylsilanyl-but-3-ynyl]-carbamic acid tert-butyl ester

: 212330-32-0
[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; for 1h; Ambient temperature;
DOI:10.1021/jo9714775

Reference yield:

: 158723-49-0,188965-46-0
(Z)-N-[(2R)-2-(tert-butoxycarbonylamino)-3-(tertbutyldiphenylsilyloxy)-propylidene]benzylamine N-oxide

: 212330-32-0
[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / tetrahydrofuran / 0.25 h / -80 °C

2: 70 percent / Bu₄NF / tetrahydrofuran / 1 h / Ambient temperature

With tetrabutyl ammonium fluoride; In tetrahydrofuran;
DOI:10.1021/jo9714775

Reference yield:

: 212330-32-0
[(1R,2R)-2-(Benzyl-hydroxy-amino)-1-hydroxymethyl-but-3-ynyl]-carbamic acid tert-butyl ester

: methyl (2S,3R)-4-acetoxy-2-(N-benzylacetoxyamino)-3-[(tert-butoxycarbonyl)amino]butanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / pyridine / CH₂Cl₂ / 1 h / Ambient temperature

2: NaIO₄, RuCl₃*H₂O / acetonitrile; CCl₄; H₂O / 0.08 h

3: diethyl ether

With pyridine; ruthenium trichloride; sodium periodate; In tetrachloromethane; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1021/jo9714775