Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester

Base Information

• Chemical Name: Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester
• CAS No.: 122594-60-9
• Molecular Formula: C₁₈H₁₆O₅
• Molecular Weight: 312.322

Synonyms:Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester

Chemical Property of Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester

Chemical Property:

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Technology Process of Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester

There total 2 articles about Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester 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:

(2R,3R)-2-acetoxy-1-(cinnamoyloxy)-3-vinylcyclohexa-3,5-diene (122594-51-8) → Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-yl ester (122594-60-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 94 percent / benzene / 15 h / 110 °C

2: 1.) O₃, 2.) dimethyl sulfide (DMS) / 1.) CH₂Cl₂, -78 deg C, 3 min, 2.) from -78 deg C to RT, 2 h

With dimethylsulfide; ozone; In benzene;

DOI:10.1021/jo00278a052

Reference yield:

(-)(1R,2R,5R,6R,7R,10S)-6-acetoxy-9-oxo-10-phenyl-5-vinyl-8-oxatricyclo<4.3.1.02,7>dec-3-ene (122594-52-9) → Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-yl ester (122594-60-9)

Guidance literature:

With dimethylsulfide; ozone; Yield given. Multistep reaction; 1.) CH₂Cl₂, -78 deg C, 3 min, 2.) from -78 deg C to RT, 2 h;

DOI:10.1021/jo00278a052

Reference yield: 85.0%

Acetic acid (1S,2R,3R,7S)-1-formyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-yl ester (122594-60-9) → Acetic acid (1R,2R,3R,7S)-1-hydroxymethyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-yl ester (122594-59-6)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 0 ℃; for 0.333333h;

DOI:10.1021/jo00278a052

upstream raw materials:

(-)(1R,2R,5R,6R,7R,10S)-6-acetoxy-9-oxo-10-phenyl-5-vinyl-8-oxatricyclo<4.3.1.0^2,7>dec-3-ene

(2R,3R)-2-acetoxy-1-(cinnamoyloxy)-3-vinylcyclohexa-3,5-diene

Downstream raw materials:

Acetic acid (1R,2R,3R,7S)-1-hydroxymethyl-5-oxo-10-phenyl-4-oxa-tricyclo[4.3.1.0^3,7]dec-8-en-2-yl ester

(-)-(1R,2R,5R,6R,7R,10S)-6-acetoxy-5-<(benzoyloxy)methyl>-9-oxo-10-phenyl-8-oxatricyclo<4.3.1.0^2,7>dec-3-ene

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