3,5-Dimethyl-benzofuran-2-carbonyl chloride

Base Information

• Chemical Name: 3,5-Dimethyl-benzofuran-2-carbonyl chloride
• CAS No.: 16817-33-7
• Molecular Formula: C11H9ClO2
• Molecular Weight: 208.64100
• DSSTox Substance ID: DTXSID70406373
• Wikidata: Q82211310
• Mol file: 16817-33-7.mol

Synonyms:3,5-Dimethyl-benzofuran-2-carbonyl chloride;16817-33-7;3,5-dimethyl-1-benzofuran-2-carbonyl chloride;3,5-Dimethylbenzofuran-2-carbonyl chloride;SCHEMBL19661814;DTXSID70406373;AKOS000293233;3,5-Dimethylbenzofuran-2-carbonylchloride

Chemical Property of 3,5-Dimethyl-benzofuran-2-carbonyl chloride

Chemical Property:

• PSA: 30.21000
• LogP: 3.42860
• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 208.0291072
• Heavy Atom Count: 14
• Complexity: 241

Purity/Quality:

98%min ^*data from raw suppliers

3,5-Dimethyl-benzofuran-2-carbonyl chloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC2=C(C=C1)OC(=C2C)C(=O)Cl

Technology Process of 3,5-Dimethyl-benzofuran-2-carbonyl chloride

There total 3 articles about 3,5-Dimethyl-benzofuran-2-carbonyl chloride 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:

3,5-dimethylbenzofuran-2-carboxylic acid (16817-32-6) → 3,5-dimethylbenzofuran-2-carbonyl chloride (16817-33-7)

Guidance literature:

With phosphorus pentachloride;

Reference yield:

p-cresol (106-44-5) → 3,5-dimethylbenzofuran-2-carbonyl chloride (16817-33-7)

Guidance literature:

Multi-step reaction with 3 steps

1: (i) aq. NaOH, (ii) H₂SO₄

2: aq. KOH

3: PCl₅

With potassium hydroxide; phosphorus pentachloride;

Reference yield:

ethyl 3,5-dimethyl-1-benzofuran-2-carboxylate (16817-31-5) → 3,5-dimethylbenzofuran-2-carbonyl chloride (16817-33-7)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. KOH

2: PCl₅

With potassium hydroxide; phosphorus pentachloride;

upstream raw materials:

3,5-dimethylbenzofuran-2-carboxylic acid

p-cresol

ethyl 3,5-dimethyl-1-benzofuran-2-carboxylate

Downstream raw materials:

(3,5-Dimethyl-benzofuran-2-yl)-(3-phenyl-ureido)-acetic acid

Benzoylamino-(3,5-dimethyl-benzofuran-2-yl)-acetic acid

3,5-dimethyl-1-benzofuran-2-carbaldehyde

Refernces

• 1、 Li, Xiang,Zhou, Bo,Yang, Run-Ze,Yang, Fu-Ming,Liang, Ren-Xiao,Liu, Ren-Rong,Jia, Yi-Xia. "Palladium-Catalyzed Enantioselective Intramolecular Dearomative Heck Reaction". supporting information. p. 13945 - 13951. Retrieved 2018/10/20.