N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide

Base Information

• Chemical Name: N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide
• CAS No.: 88303-19-9
• Molecular Formula: C11H16FNO2S
• Molecular Weight: 245.318
• DSSTox Substance ID: DTXSID80455493
• Wikidata: Q82277539
• Mol file: 88303-19-9.mol

Synonyms:88303-19-9;N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide;Benzenesulfonamide, N-(1,1-dimethylethyl)-2-fluoro-4-methyl-;N-(tert-butyl)-2-fluoro-4-methylbenzenesulfonamide;SCHEMBL1794606;DTXSID80455493;MNIVNHPFRQXPJP-UHFFFAOYSA-N;MFCD26392609;N-t-Butyl-2-fluoro-4-methyl-benzenesulfonamide

Chemical Property of N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide

Chemical Property:

• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 245.08857809
• Heavy Atom Count: 16
• Complexity: 329

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(C=C1)S(=O)(=O)NC(C)(C)C)F

Technology Process of N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide

There total 4 articles about N-tert-butyl-2-fluoro-4-methylbenzenesulfonamide 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: 74.0%

N-t-butyl-p-toluenesulfonamide (2849-81-2) → N-(tert-butyl)-2-fluoro-4-methylbenzenesulfonamide (88303-19-9)

Guidance literature:

N-t-butyl-p-toluenesulfonamide; With n-butyllithium; In tetrahydrofuran; hexane; for 2h;

With N-fluorobis(benzenesulfon)imide; In tetrahydrofuran; hexane; for 3h; Further stages.;

DOI:10.1021/jm010484p

Reference yield: 55.0%

N-t-butyl-p-toluenesulfonamide (2849-81-2) → N-(tert-butyl)-2-fluoro-4-methylbenzenesulfonamide (88303-19-9)

Guidance literature:

In tetrahydrofuran; toluene; Ambient temperature;

DOI:10.1021/ja00314a050

Reference yield: 52.0%

N-fluoro-N-(exo-2-norbornyl)-p-toluenesulfonamide (103731-48-2) + N-t-butyl-p-toluenesulfonamide (2849-81-2) → N-(tert-butyl)-2-fluoro-4-methylbenzenesulfonamide (88303-19-9)

Guidance literature:

In tetrahydrofuran; hexane; toluene;

upstream raw materials:

N-t-butyl-p-toluenesulfonamide

N-fluoro-N-(exo-2-norbornyl)-p-toluenesulfonamide

2-fluoro-4-methylbenzene-1-sulfonyl chloride

tert-butylamine

Downstream raw materials:

N-tert-butyl-4-bromomethyl-2-fluorobenzenesulfonamide