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5-(1-Hydroxytridecyl)oxolan-2-one

Base Information Edit
  • Chemical Name:5-(1-Hydroxytridecyl)oxolan-2-one
  • CAS No.:134698-86-5
  • Molecular Formula:C17H32 O3
  • Molecular Weight:284.439
  • Hs Code.:
  • Wikidata:Q105285428
  • Metabolomics Workbench ID:48305
  • Mol file:134698-86-5.mol
5-(1-Hydroxytridecyl)oxolan-2-one

Synonyms:5-(1-hydroxytridecyl)oxolan-2-one;(5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-one;LMFA05000682

Suppliers and Price of 5-(1-Hydroxytridecyl)oxolan-2-one
Supply Marketing:Edit
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 3 raw suppliers
Chemical Property of 5-(1-Hydroxytridecyl)oxolan-2-one Edit
Chemical Property:
  • Vapor Pressure:4.42E-09mmHg at 25°C 
  • Boiling Point:427°C at 760 mmHg 
  • Flash Point:169.3°C 
  • PSA:46.53000 
  • Density:0.977g/cm3 
  • LogP:4.36390 
  • XLogP3:5.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:12
  • Exact Mass:284.23514488
  • Heavy Atom Count:20
  • Complexity:253
Purity/Quality:

98%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCC(C1CCC(=O)O1)O
Technology Process of 5-(1-Hydroxytridecyl)oxolan-2-one

There total 1 articles about 5-(1-Hydroxytridecyl)oxolan-2-one 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 98 percent / MnO2 / hexane / 24 h / 20 °C
2: 93 percent / 18-crown-6; t-BuOK / tetrahydrofuran / 2.5 h / -78 °C
3: 86 percent / OsO4; MeSO2NH2; (DHQD)2PHAL / K3Fe(CN)6; K2CO3 / 2-methyl-propan-2-ol; H2O / 0 °C
4: 98 percent / H2 / Pd/C / methanol / 24 h / 760 Torr
With manganese(IV) oxide; osmium(VIII) oxide; 18-crown-6 ether; methanesulfonamide; potassium tert-butylate; hydrogen; 1,4-bis(9-O-dihydroquinidine)phthalazine; palladium on activated charcoal; potassium carbonate; potassium hexacyanoferrate(III); In tetrahydrofuran; methanol; hexane; water; tert-butyl alcohol; 2: Still-Gennari reaction / 3: Sharpless asymmetric dihydroxylation;
DOI:10.1021/jo061057s
Guidance literature:
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1055/s-0036-1590858
Guidance literature:
Multi-step reaction with 19 steps
1: i-Pr2NEt / CH2Cl2
2: DIBAL / CH2Cl2
3: 76 percent / NaH / tetrahydrofuran / -78 °C
4: PPTS / CH2Cl2
5: AD-mix α, CH3SO2NH2 / 2-methyl-propan-2-ol; H2O
6: PPTS / CH2Cl2
7: LiAlH4 / diethyl ether
8: pyridine
9: PPTS / methanol
10: KOH
11: 98 percent / PPTS / CH2Cl2
12: 96 percent / BF3*Et2O / tetrahydrofuran
13: i-Pr2NEt / CH2Cl2
14: PPTS / methanol
15: 53 percent / CuI, pyrrolidine / Pd(Ph3P)4
16: 77 percent / H2 / Rh(Ph3P)3Cl / benzene
17: Et3N / CH2Cl2
18: HCl / methanol
19: KOH / tetrahydrofuran
With pyrrolidine; pyridine; hydrogenchloride; potassium hydroxide; AD-mix-α; copper(l) iodide; lithium aluminium tetrahydride; methanesulfonamide; boron trifluoride diethyl etherate; hydrogen; pyridinium p-toluenesulfonate; sodium hydride; diisobutylaluminium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; Wilkinson's catalyst; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; tert-butyl alcohol; benzene;
DOI:10.1016/0040-4039(96)01086-6
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