m-isopropylphenyl acetate

Base Information

• Chemical Name: m-isopropylphenyl acetate
• CAS No.: 36438-57-0
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.231
• Mol file: 36438-57-0.mol

Synonyms:m-isopropylphenyl acetate

Chemical Property of m-isopropylphenyl acetate

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Technology Process of m-isopropylphenyl acetate

There total 4 articles about m-isopropylphenyl acetate 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: 92.6%

3-isopropylhydroxybenzene (618-45-1) + acetyl chloride (75-36-5) → m-isopropylphenyl acetate (36438-57-0)

Guidance literature:

3-isopropylhydroxybenzene; With pyridine; In dichloromethane; at 29 ℃; for 0.25h;

acetyl chloride; In dichloromethane; at 20 ℃;

Reference yield: 4.3%

Isopropylbenzene (98-82-8) + acetic anhydride (108-24-7) → 4-isopropylphenyl acetate (2664-32-6) + m-isopropylphenyl acetate (36438-57-0) + 2-isopropyl-phenyl acetate (1608-68-0) + acetophenone (98-86-2)

Guidance literature:

With ferrous perchlorate; dihydrogen peroxide; acetonitrile; at 30 ℃; Product distribution;

Reference yield:

acetic acid-(3-isopropenyl-phenyl ester) (51985-05-8) → m-isopropylphenyl acetate (36438-57-0)

Guidance literature:

With ethanol; platinum; Hydrogenation;

DOI:10.1021/jo01372a011

upstream raw materials:

acetic acid-(3-isopropenyl-phenyl ester)

Isopropylbenzene

acetic anhydride

3-isopropylhydroxybenzene

Downstream raw materials:

1-(2-hydroxy-4-isopropylphenyl)ethanone

3-isopropylhydroxybenzene

Refernces

• 1、 -. "Tetrahydronaphthalene derivates, processes for preparing them and their use as antiinflammatory agents". Page/Page column 56. . Retrieved 2010/11/28.