2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

Base Information

Chemical Name:2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol
CAS No.:287194-56-3
Molecular Formula:C₂₉H₃₄O₅S
Molecular Weight:494.652
Hs Code.:

Synonyms:2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

Suppliers and Price of 2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

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 2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

There total 12 articles about 2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-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: 84.0%

: 6228-98-4
phenylthioacetylene

: 272787-63-0
2-benzyloxy-6-methyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-one

: 287194-56-3
2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

Guidance literature:: With n-butyllithium; In tetrahydrofuran; at -78 - 0 ℃;

Reference yield:

: 100-39-0
benzyl bromide

: 287194-56-3
2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

Guidance literature:: Multi-step reaction with 10 steps

1: 82 percent / NaH / dimethylformamide / -40 - 20 °C

2: 80 percent / NMO; OsO₄ / acetone; H₂O / 20 °C

3: 93 percent / TsOH*H₂O / 0.33 h / 20 °C

4: 96 percent / TBAF / tetrahydrofuran / 2 h / 20 °C

5: 100 percent / Et₃N; SO₃*Py / dimethylsulfoxide / 0.17 h / 20 °C

6: 98 percent / 80 percent aq. AcOH / 20 °C

7: 77 percent / Br₂; NaOAc / dimethylformamide / 0.5 h / 0 - 20 °C

8: 67 percent / CH₂Cl₂ / Heating

9: 88 percent / n-Bu₃SnH / toluene / 0.17 h / Heating

10: 84 percent / n-BuLi / tetrahydrofuran; hexane / -78 - 0 °C

With osmium(VIII) oxide; n-butyllithium; N-methyl-2-indolinone; pyridine-SO₃ complex; tetrabutyl ammonium fluoride; bromine; tri-n-butyl-tin hydride; sodium acetate; sodium hydride; toluene-4-sulfonic acid; acetic acid; triethylamine; In tetrahydrofuran; hexane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone; toluene; 1: Alkylation / 2: Oxidation / 3: Cyclization / 4: desilylation / 5: Oxidation / 6: Hydrolysis / 7: Oxidation / 8: Esterification / 9: Elimination / 10: Addition;
DOI:10.1016/S0040-4020(00)00467-1

Reference yield:

: 272787-60-7
2-benzyloxy-3-(2,2,11-trimethyldecahydro-1,3,5,9-tetraoxabenzo[a]cyclopenta[e]cycloocten-4-yl)propionaldehyde

: 287194-56-3
2-benzyloxy-6-methyl-3-phenylsulfanylethynyldodecahydro-4,8,12-trioxadibenzo[a,d]cyclooctene-3-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / 80 percent aq. AcOH / 20 °C

2: 77 percent / Br₂; NaOAc / dimethylformamide / 0.5 h / 0 - 20 °C

3: 67 percent / CH₂Cl₂ / Heating

4: 88 percent / n-Bu₃SnH / toluene / 0.17 h / Heating

5: 84 percent / n-BuLi / tetrahydrofuran; hexane / -78 - 0 °C

With n-butyllithium; bromine; tri-n-butyl-tin hydride; sodium acetate; acetic acid; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; 1: Hydrolysis / 2: Oxidation / 3: Esterification / 4: Elimination / 5: Addition;
DOI:10.1016/S0040-4020(00)00467-1