3-methylindyl acetate

Base Information

• Chemical Name: 3-methylindyl acetate
• CAS No.: 81707-12-2
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.242
• Mol file: 81707-12-2.mol

Synonyms:

Chemical Property of 3-methylindyl acetate

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Technology Process of 3-methylindyl acetate

There total 4 articles about 3-methylindyl 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: 29.0%

1-(2-chlorophenyl)-3-butenyl acetate → 1-methylindane (767-58-8) + 1-phenylbut-3-enyl acetate (132587-07-6,132587-15-6,2833-34-3) + 3-methylindyl acetate (81707-10-0,81707-12-2) + 3-methylindyl acetate (81707-10-0,81707-12-2)

Guidance literature:

With potassium bromide; Ni(1,4,8,11-tetraazacyclotetradecane)Br₂; In N,N-dimethyl-formamide; at 25 ℃; Electrochemical reaction;

DOI:10.1055/s-2006-948182

Reference yield: 29.0%

1-(2-chlorophenyl)-3-butenyl acetate → 1-methylindane (767-58-8) + 1-phenylbut-3-enyl acetate (132587-07-6,132587-15-6,2833-34-3) + 3-methylindyl acetate (81707-10-0,81707-12-2) + 3-methylindyl acetate (81707-10-0,81707-12-2)

Guidance literature:

With potassium bromide; Ni(1,4,8,11-tetraazacyclotetradecane)Br₂; In N,N-dimethyl-formamide; at 25 ℃; Electrochemical reaction;

DOI:10.1055/s-2006-948182

Reference yield: 2.0%

C12H13BrO2 → 1-phenylbut-3-enyl acetate (132587-07-6,132587-15-6,2833-34-3) + 3-methylindyl acetate (81707-10-0,81707-12-2) + 3-methylindyl acetate (81707-10-0,81707-12-2)

Guidance literature:

With potassium bromide; Ni(tmc)Br₂; In N,N-dimethyl-formamide; at 25 ℃; Title compound not separated from byproducts.; Electrochemical reaction;

DOI:10.1055/s-2006-948182