(5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone

Base Information

• Chemical Name: (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone
• CAS No.: 200621-10-9
• Molecular Formula: C₁₁H₁₅BrO
• Molecular Weight: 243.143
• Mol file: 200621-10-9.mol

Synonyms:(5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone

Chemical Property of (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone

There total 3 articles about (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone 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%

(R)-6-methylcarvone (138812-34-7) + acetic acid (64-19-7,77671-22-8) → (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone (200621-10-9) + 2,6-Dimethyl-5-(2-acetoxy-1-bromoisopropyl)cyclohexenone

Guidance literature:

With N-Bromosuccinimide; sodium acetate; In dichloromethane; at 0 - 20 ℃; for 6h;

DOI:10.1039/a706321k

Reference yield: 20.0%

(R)-6-methylcarvone (138812-34-7) → (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone (200621-10-9) + 2,6-Dimethyl-5-(2-acetoxy-1-bromoisopropyl)cyclohexenone

Guidance literature:

With N-Bromosuccinimide; sodium acetate; acetic acid; In dichloromethane; at 0 - 20 ℃; for 6h;

DOI:10.1039/a706321k

Reference yield:

(R)-Carvone (6485-40-1,2244-16-8) → (5R,6RS)-5-(3-bromoprop-1-en-2-yl)-2,6-dimethylcyclohex-2-enone (200621-10-9)

Guidance literature:

Multi-step reaction with 2 steps

1: LDA / tetrahydrofuran / 1.) -10 deg C to r.t., 2.) 9 h

2: 60 percent / NBS, NaOAc, AcOH / CH₂Cl₂ / 6 h / 0 - 20 °C

With N-Bromosuccinimide; sodium acetate; acetic acid; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane;

DOI:10.1039/a706321k

upstream raw materials:

(R)-6-methylcarvone

acetic acid

(R)-Carvone