Butane-1,2,3,4-tetrol

Base Information

• Chemical Name: Butane-1,2,3,4-tetrol
• CAS No.: 7541-59-5
• Molecular Formula: C₄H₁₀O₄
• Molecular Weight: 122.121
• European Community (EC) Number: 205-737-3,231-418-3,621-282-7,625-103-3,626-535-5
• NSC Number: 20660
• DSSTox Substance ID: DTXSID70859289
• Nikkaji Number: J307.870A
• Wikidata: Q81986208
• Metabolomics Workbench ID: 133697
• ChEMBL ID: CHEMBL402812
• Mol file: 7541-59-5.mol

Synonyms:tetritol

Chemical Property of Butane-1,2,3,4-tetrol

Chemical Property:

• PSA: 80.92000
• LogP: -2.30720
• XLogP3: -2.3
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 122.05790880
• Heavy Atom Count: 8
• Complexity: 48

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Alcohols and Polyols, Other
• Canonical SMILES: C(C(C(CO)O)O)O

Technology Process of Butane-1,2,3,4-tetrol

There total 27 articles about Butane-1,2,3,4-tetrol 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: 99.0%

cis-2,3-epoxy-1,4-butanediol (4440-87-3,63621-92-1) → 1,2,3,4-butanetetrol (2319-57-5,2418-52-2,6968-16-7,7493-90-5,7541-59-5,10030-58-7,188346-77-2,149-32-6)

Guidance literature:

With water; at 100 ℃; for 9h;

DOI:10.1021/jo702401t

Reference yield: 60.0%

1,4-butenediol (821-11-4,6117-80-2,110-64-5) → 1,2,3,4-butanetetrol (2319-57-5,2418-52-2,6968-16-7,7493-90-5,7541-59-5,10030-58-7,188346-77-2,149-32-6)

Guidance literature:

With potassium permanganate; dihydrogen peroxide; In water; acetone; at 0 ℃; for 2h; Temperature; Inert atmosphere; Green chemistry;

DOI:10.1039/c5ra01646k

Reference yield: 53.6%

cellulose (9004-34-6) → 1,2,3,4-butanetetrol (2319-57-5,2418-52-2,6968-16-7,7493-90-5,7541-59-5,10030-58-7,188346-77-2,149-32-6) + ethylene glycol (107-21-1)

Guidance literature:

With ruthenium-carbon composite; hydrogen; In water; at 215 ℃; for 1.5h; under 39003.9 Torr; Reagent/catalyst; Catalytic behavior; Autoclave;

DOI:10.1039/c6ra27524a

upstream raw materials:

1,4-dibromo-2-butene

D-erythrose

buta-1,3-diene

formaldehyd

Downstream raw materials:

formic acid

meso-2,2'-diphenyl-tetrahydro-[4,4']bi[1,3,2]dioxaborolyl

2,2'-diethyl-tetrahydro-[4,4']bi[1,3,2]dioxaborolyl

1,2,3,4-tetrakis-formyloxy-butane

Refernces

• 1、 Gumina, Bianca,Mauriello, Francesco,Pietropaolo, Rosario,Galvagno, Signorino,Espro, Claudia. "Hydrogenolysis of sorbitol into valuable C3-C2 alcohols at low H2 pressure promoted by the heterogeneous Pd/Fe3O4 catalyst". . p. 152 - 160. Retrieved 2018/02/17.
• 2、 Dalmizrak, Di?dem,G?ksu, Haydar,Gültekin, Mehmet Serdar. "A facile synthesis of vicinal cis-diols from olefins catalyzed by in situ generated MnxOy nanoaggregates". . p. 20751 - 20755. Retrieved 2015/03/18.