2-[3-(Benzenesulfonyl)propoxy]oxane

Base Information

Chemical Name:2-[3-(Benzenesulfonyl)propoxy]oxane
CAS No.:95791-15-4
Molecular Formula:C14H20O4S
Molecular Weight:284.376
Hs Code.:
DSSTox Substance ID:DTXSID20552935
Mol file:95791-15-4.mol

Synonyms:95791-15-4;2-[3-(Benzenesulfonyl)propoxy]oxane;DTXSID20552935

Suppliers and Price of 2-[3-(Benzenesulfonyl)propoxy]oxane

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-[3-(Benzenesulfonyl)propoxy]oxane

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:284.10823029
Heavy Atom Count:19
Complexity:341

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCOC(C1)OCCCS(=O)(=O)C2=CC=CC=C2

Technology Process of 2-[3-(Benzenesulfonyl)propoxy]oxane

There total 4 articles about 2-[3-(Benzenesulfonyl)propoxy]oxane 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: 85.0%

: 111086-99-8
2-(3-Phenylsulfanyl-propoxy)-tetrahydro-pyran

: 95791-15-4
1-(phenylsulfonyl)-3-<(tetrahydropyranyl)oxy>propane

Guidance literature:: With tetra-n-butylammonium peroxomonosulfate; sodium carbonate; In dichloromethane; for 48h; Ambient temperature;
DOI:10.1021/jo00238a011

Reference yield:

: 33821-94-2
3-(tetrahydro-2H-pyran-2-yloxy)propyl bromide

: 95791-15-4
1-(phenylsulfonyl)-3-<(tetrahydropyranyl)oxy>propane

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / DBU / benzene / 4 h / Ambient temperature

2: 85 percent / sodium carbonate, tetra-n-butylammonium oxone (TBA-OX) / CH₂Cl₂ / 48 h / Ambient temperature

With tetra-n-butylammonium peroxomonosulfate; sodium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; benzene;
DOI:10.1021/jo00238a011

Reference yield:

: 108-98-5
thiophenol

: 95791-15-4
1-(phenylsulfonyl)-3-<(tetrahydropyranyl)oxy>propane

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / DBU / benzene / 4 h / Ambient temperature

2: 85 percent / sodium carbonate, tetra-n-butylammonium oxone (TBA-OX) / CH₂Cl₂ / 48 h / Ambient temperature

With tetra-n-butylammonium peroxomonosulfate; sodium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; benzene;
DOI:10.1021/jo00238a011