(6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol

Base Information

• Chemical Name: (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol
• CAS No.: 120467-11-0
• Molecular Formula: C₂₄H₂₈O₂
• Molecular Weight: 348.485
• Mol file: 120467-11-0.mol

Synonyms:(6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol

Chemical Property of (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol

There total 6 articles about (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol 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: 72.0%

dihydropinosylvin (14531-52-3) + (+)-p-menthadiene-3-ol (491-05-4,4017-76-9,4017-77-0,65733-29-1,65733-30-4,74410-00-7,96555-02-1,115362-62-4,141316-25-8) → (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol (120467-11-0)

Guidance literature:

With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.25h; diastereoselective reaction; Inert atmosphere;

DOI:10.1039/c4cc08562k

Reference yield: 9.0%

dihydropinosylvin (14531-52-3) + (1S,4R)-p-mentha-2,8-dien-1-ol (22972-51-6) → (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol (120467-11-0)

Guidance literature:

With toluene-4-sulfonic acid; In benzene; at 45 ℃; for 2h;

DOI:10.1039/P19880001263

Reference yield:

1,3-dimethoxy-5-(2-phenylethyl)benzene (78916-50-4) → (6aR,10aR)-6,6,9-trimethyl-3-phenethyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-ol (120467-11-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 71 percent / BBr₃ / CH₂Cl₂ / 1.) -70 deg C, 2.) room temp., 2 h

2: 9 percent / toluene-p-sulphonic acid / benzene / 2 h / 45 °C

With boron tribromide; toluene-4-sulfonic acid; In dichloromethane; benzene;

DOI:10.1039/P19880001263

upstream raw materials:

dihydropinosylvin

(1S,4R)-p-mentha-2,8-dien-1-ol

1,3-dimethoxy-5-(2-phenylethyl)benzene

D-limonene