(3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Base Information

Chemical Name:(3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one
CAS No.:206058-80-2
Molecular Formula:C₂₅H₂₆O₇
Molecular Weight:438.477
Hs Code.:

Synonyms:(3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Suppliers and Price of (3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

There total 5 articles about (3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one 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: 97.0%

: 100-39-0
benzyl bromide

: 206058-79-9
(3S,4R)-10-Hydroxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

: 206058-80-2
(3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Guidance literature:: With potassium carbonate; In acetone; at 55 ℃; for 7h;
DOI:10.7164/antibiotics.51.383

Reference yield:

: 6110-37-8
methyl 2,4-dimethoxy-6-methylbenzoate

: 206058-80-2
(3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / LDA / tetrahydrofuran / 4.5 h / -78 - 0 °C

2: 89 percent / cyclohexene / 10 percent Pd-C / toluene / 12 h / 20 °C

3: 97 percent / K₂CO₃ / acetone / 7 h / 55 °C

With potassium carbonate; lithium diisopropyl amide; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; acetone; toluene; 1: Cycloaddition / 2: Aromatisation / 3: Etherification;
DOI:10.7164/antibiotics.51.383

Reference yield:

: 54826-92-5
(5R,6S)-5,6-dihydro-5-hydroxy-6-methylpyran-2-one

: 206058-80-2
(3S,4R)-10-Benzyloxy-7,9-dimethoxy-4-methoxymethoxy-3-methyl-3,4-dihydro-benzo[g]isochromen-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / P₂O₅ / CH₂Cl₂ / 0.25 h / 20 °C

2: 85 percent / LDA / tetrahydrofuran / 4.5 h / -78 - 0 °C

3: 89 percent / cyclohexene / 10 percent Pd-C / toluene / 12 h / 20 °C

4: 97 percent / K₂CO₃ / acetone / 7 h / 55 °C

With phosphorus pentoxide; potassium carbonate; lithium diisopropyl amide; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetone; toluene; 1: Substitution / 2: Cycloaddition / 3: Aromatisation / 4: Etherification;
DOI:10.7164/antibiotics.51.383