Cyclopentanol, 1-(1,1-dimethylethyl)-

Base Information

Chemical Name:Cyclopentanol, 1-(1,1-dimethylethyl)-
CAS No.:69745-48-8
Molecular Formula:C9H18O
Molecular Weight:142.241
Hs Code.:
DSSTox Substance ID:DTXSID40463630
Nikkaji Number:J1.934.229H
Wikidata:Q82288609

Synonyms:Cyclopentanol, 1-(1,1-dimethylethyl)-;69745-48-8;1-tert-butylcyclopentan-1-ol;Cyclopentanol,1-(1,1-dimethylethyl)-;SCHEMBL12971961;DTXSID40463630;AKOS015282714

Suppliers and Price of Cyclopentanol, 1-(1,1-dimethylethyl)-

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 7 raw suppliers

Chemical Property of Cyclopentanol, 1-(1,1-dimethylethyl)-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:142.135765193
Heavy Atom Count:10
Complexity:115

Purity/Quality:: 99%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1(CCCC1)O

Technology Process of Cyclopentanol, 1-(1,1-dimethylethyl)-

There total 6 articles about Cyclopentanol, 1-(1,1-dimethylethyl)- 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:

: dimethyl 2-cyclopentyl-2-methylmalonate

: 5581-94-2
3-tert-Butyl-cyclopentanone

: 40557-24-2
2-tert-butylcyclopentanone

: 69745-48-8
1-tert-butyl-cyclopentanol

Guidance literature:: Multi-step reaction with 4 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 19 h / 0 - 20 °C / Inert atmosphere

2: pyridine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

3: lithium triethylborohydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

4: oxygen; bis(1-methyl-1-phenylethyl)peroxide / chlorobenzene / 9 h / 25 °C / UV-irradiation

With pyridine; lithium aluminium tetrahydride; bis(1-methyl-1-phenylethyl)peroxide; oxygen; lithium triethylborohydride; In tetrahydrofuran; dichloromethane; chlorobenzene;
DOI:10.1021/acs.joc.1c00902

Reference yield:

: 1125-23-1
2-cyclopentyl-2-methylpropane-1,3-diol

: 5581-94-2
3-tert-Butyl-cyclopentanone

: 40557-24-2
2-tert-butylcyclopentanone

: 69745-48-8
1-tert-butyl-cyclopentanol

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

2: lithium triethylborohydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

3: oxygen; bis(1-methyl-1-phenylethyl)peroxide / chlorobenzene / 9 h / 25 °C / UV-irradiation

With pyridine; bis(1-methyl-1-phenylethyl)peroxide; oxygen; lithium triethylborohydride; In tetrahydrofuran; dichloromethane; chlorobenzene;
DOI:10.1021/acs.joc.1c00902

Reference yield:

: 2-cyclopentyl-2-methylpropane-1,3-diyl bis-(trifluoromethanesulfonate)

: 5581-94-2
3-tert-Butyl-cyclopentanone

: 40557-24-2
2-tert-butylcyclopentanone

: 69745-48-8
1-tert-butyl-cyclopentanol

Guidance literature:: Multi-step reaction with 2 steps

1: lithium triethylborohydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

2: oxygen; bis(1-methyl-1-phenylethyl)peroxide / chlorobenzene / 9 h / 25 °C / UV-irradiation

With bis(1-methyl-1-phenylethyl)peroxide; oxygen; lithium triethylborohydride; In tetrahydrofuran; chlorobenzene;
DOI:10.1021/acs.joc.1c00902