moenocinol benzyl ether

Base Information

Chemical Name:moenocinol benzyl ether
CAS No.:87957-22-0
Molecular Formula:C₃₂H₄₈O
Molecular Weight:448.733
Hs Code.:

Synonyms:moenocinol benzyl ether

Suppliers and Price of moenocinol benzyl ether

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 moenocinol benzyl ether

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of moenocinol benzyl ether

There total 19 articles about moenocinol benzyl ether 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:

: 5389-87-7
1-chloro-3,7-dimethylocta-2,6-diene

: 87957-22-0
moenocinol benzyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / 1.5M-n-BuLi / hexane; tetrahydrofuran

2: 1.) lithium di-isopropylamide, 2.) hexamethylphosphoric triamide, 3.) n-Bu₄NF*3H₂O

With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; tetrabutyl ammonium fluoride; lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1039/P19830001777

Reference yield:

: 73199-55-0
(Z)-3-Benzenesulfonyl-8-benzyloxy-2,6-dimethyl-oct-6-en-2-ol

: 87957-22-0
moenocinol benzyl ether

Guidance literature:: Multi-step reaction with 8 steps

1: 3.10 g / KOH / methanol / 1 h / Heating

2: 90 percent / 1.43M-n-BuLi / tetrahydrofuran; hexane / 1.) -78 deg C, 20 min, 2.) room temperature, 2.5 h

3: 85 percent / 5.65percent Na(Hg) / tetrahydrofuran; methanol / 135.84 h / 20 °C

4: 100 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

5: 98 percent / NaI / acetone / 16 h / Heating

6: 83 percent / 1.5M-n-BuLi / tetrahydrofuran / 3 h / Ambient temperature

7: 85 percent / 1.5M-n-BuLi / hexane; tetrahydrofuran

8: 1.) lithium di-isopropylamide, 2.) hexamethylphosphoric triamide, 3.) n-Bu₄NF*3H₂O

With N,N,N,N,N,N-hexamethylphosphoric triamide; potassium hydroxide; n-butyllithium; sodium amalgam; tetrabutyl ammonium fluoride; triethylamine; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane; acetone;
DOI:10.1039/P19830001777

Reference yield:

: 73199-56-1
(Z)-1-benzyloxy-6-phenylsulphonyl-3-methylhex-2-ene

: 87957-22-0
moenocinol benzyl ether

Guidance literature:: Multi-step reaction with 7 steps

1: 90 percent / 1.43M-n-BuLi / tetrahydrofuran; hexane / 1.) -78 deg C, 20 min, 2.) room temperature, 2.5 h

2: 85 percent / 5.65percent Na(Hg) / tetrahydrofuran; methanol / 135.84 h / 20 °C

3: 100 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

4: 98 percent / NaI / acetone / 16 h / Heating

5: 83 percent / 1.5M-n-BuLi / tetrahydrofuran / 3 h / Ambient temperature

6: 85 percent / 1.5M-n-BuLi / hexane; tetrahydrofuran

7: 1.) lithium di-isopropylamide, 2.) hexamethylphosphoric triamide, 3.) n-Bu₄NF*3H₂O

With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; sodium amalgam; tetrabutyl ammonium fluoride; triethylamine; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane; acetone;
DOI:10.1039/P19830001777