1-(Benzenesulfonyl)bicyclo[1.1.0]butane

Base Information

• Chemical Name: 1-(Benzenesulfonyl)bicyclo[1.1.0]butane
• CAS No.: 80989-84-0
• Molecular Formula: C10H10O2S
• Molecular Weight: 194.254
• DSSTox Substance ID: DTXSID30508706
• Wikidata: Q82365846

Synonyms:80989-84-0;1-(Benzenesulfonyl)bicyclo[1.1.0]butane;Bicyclo[1.1.0]butane, 1-(phenylsulfonyl)-;1-(phenylsulfonyl)bicyclo[1.1.0]butane;SCHEMBL22026800;DTXSID30508706;AKOS037645968;AS-65272;1-(benzenesulfonyl)-bicyclo[1.1.0]butane

Chemical Property of 1-(Benzenesulfonyl)bicyclo[1.1.0]butane

Chemical Property:

• XLogP3: 1.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 194.04015073
• Heavy Atom Count: 13
• Complexity: 313

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C2C1(C2)S(=O)(=O)C3=CC=CC=C3

Technology Process of 1-(Benzenesulfonyl)bicyclo[1.1.0]butane

There total 11 articles about 1-(Benzenesulfonyl)bicyclo[1.1.0]butane 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: 60.0%

4-(-phenylsulfonyl)-1,2-epoxybutane (81582-94-7) → 1-(phenylsulfonyl)bicyclo[1.1.0]butane (80989-84-0)

Guidance literature:

With n-butyllithium; methanesulfonyl chloride; In tetrahydrofuran; hexane; for 0.166667h; ice-cooled temp.;

DOI:10.1016/S0040-4020(01)80112-5

Reference yield: 60.0%

Methanesulfonic acid (1S,2R)-2-benzenesulfonyl-cyclopropylmethyl ester (81599-94-2) → 1-(phenylsulfonyl)bicyclo[1.1.0]butane (80989-84-0)

Guidance literature:

With n-butyllithium; In tetrahydrofuran; for 0.0833333h;

DOI:10.1021/jo00134a012

Reference yield: 55.0%

Methanesulfonic acid 2-benzenesulfonyl-cyclopropylmethyl ester (157893-57-7) → 1-Phenylsulfonylbicyclo<1.1.0>butane (80989-84-0)

Guidance literature:

With n-butyllithium;

DOI:10.1016/S0040-4039(01)82950-6

upstream raw materials:

4-(-phenylsulfonyl)-1,2-epoxybutane

Methanesulfonic acid (1S,2R)-2-benzenesulfonyl-cyclopropylmethyl ester

Methanesulfonic acid 2-benzenesulfonyl-cyclopropylmethyl ester

(but-3-en-1-ylsulfonyl)benzene

Downstream raw materials:

2-(3-Benzenesulfonyl-bicyclo[1.1.0]but-1-yl)-ethanol

(3-Methyl-cyclobutanesulfonyl)-benzene

(3-Benzenesulfonyl-bicyclo[1.1.0]but-1-yl)-methanol

C₁₆H₁₆O₂SSe

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