2,2,3-Trimethylbutan-1-ol

Base Information

• Chemical Name: 2,2,3-Trimethylbutan-1-ol
• CAS No.: 55505-23-2
• Molecular Formula: 55505-23-2
• Molecular Weight: 116.203
• Hs Code.: 2905199090
• European Community (EC) Number: 815-336-0
• DSSTox Substance ID: DTXSID60595861
• Wikidata: Q82490958

Synonyms:2,2,3-Trimethylbutan-1-ol;55505-23-2;2,2,3-TRIMETHYL-1-BUTANOL;2,2,3-trimethyl-butanol;SCHEMBL1985873;DTXSID60595861;FAMOAJMEFGYSNY-UHFFFAOYSA-N;AKOS018649905;EN300-179652

Chemical Property of 2,2,3-Trimethylbutan-1-ol

Chemical Property:

• PSA: 20.23000
• LogP: 1.66090
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 116.120115130
• Heavy Atom Count: 8
• Complexity: 64.8

Purity/Quality:

99% ^*data from raw suppliers

2,2,3-trimethylbutan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)C(C)(C)CO

Technology Process of 2,2,3-Trimethylbutan-1-ol

There total 15 articles about 2,2,3-Trimethylbutan-1-ol 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: 80.0%

2-(1,1,2-trimethylpropyl)[1,3,2]dioxaborolane (99810-77-2) + 1,1-dibromomethane (74-95-3) → 2,3-dimethylbutan-2-ol (594-60-5) + 2,2,3-trimethylbutan-1-ol (55505-23-2)

Guidance literature:

2-(1,1,2-trimethylpropyl)[1,3,2]dioxaborolane; 1,1-dibromomethane; With n-butyllithium; In tetrahydrofuran; hexane; at 20 ℃; for 2h; Cooling with acetone-dry ice; Inert atmosphere;

With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; hexane; water; at 0 - 20 ℃;

DOI:10.1021/jo4000459

Reference yield: 80.0%

(dimethoxy)thexyl borane (56118-62-8) + 1,1-dibromomethane (74-95-3) → 2,3-dimethylbutan-2-ol (594-60-5) + 2,2,3-trimethylbutan-1-ol (55505-23-2)

Guidance literature:

(dimethoxy)thexyl borane; 1,1-dibromomethane; With n-butyllithium; In tetrahydrofuran; hexane; at 20 ℃; for 2h; Cooling with acetone-dry ice; Inert atmosphere;

With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; hexane; water; at 0 - 20 ℃;

DOI:10.1021/jo4000459

Reference yield: 80.0%

2-(1,1,2-trimethylpropyl)-1,3-dioxaborinane (63689-74-7) + 1,1-dibromomethane (74-95-3) → 2,3-dimethylbutan-2-ol (594-60-5) + 2,2,3-trimethylbutan-1-ol (55505-23-2)

Guidance literature:

2-(1,1,2-trimethylpropyl)-1,3-dioxaborinane; 1,1-dibromomethane; With n-butyllithium; In tetrahydrofuran; hexane; at 20 ℃; for 2h; Cooling with acetone-dry ice; Inert atmosphere;

With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; hexane; water; at 0 - 20 ℃;

DOI:10.1021/jo4000459

upstream raw materials:

4,4,5,5-tetramethyl-[1,3]dioxane

2,2,3-trimethylbutanoic acid

2,2,3-trimethylbutansaeuremethylester

methanol

Downstream raw materials:

triptane

Phenyl-(2,2,3-trimethyl-butoxysulfonyl)-acetic acid

1-bromo-2,2,3-trimethylbutane

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