((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

Base Information

Chemical Name:((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol
CAS No.:1374851-82-7
Molecular Formula:C₃₀H₃₇FO₄Si
Molecular Weight:508.705
Hs Code.:

Synonyms:((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

Suppliers and Price of ((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

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 ((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

There total 11 articles about ((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol 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:

: C₃₀H₃₅FO₄Si

: 1374851-82-7
((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

Guidance literature:: With methanol; sodium tetrahydroborate; at 0 ℃; for 1h;
DOI:10.1016/j.tet.2012.03.023

Reference yield:

: 1009810-90-5
2,3-(cyclopentylidenedioxy)-4-vinylcyclopentanol

: 1374851-82-7
((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C

1.2: 3 h / 0 - 20 °C

2.1: hydrogenchloride / methanol / 25 °C

3.1: 1H-imidazole; dmap / dichloromethane / 2 h / 0 - 20 °C

4.1: pyridine; diethylamino-sulfur trifluoride / dichloromethane / 12 h / 20 °C / Inert atmosphere

5.1: sodium periodate; osmium(VIII) oxide; water; 4-methylmorpholine N-oxide / methanol / 2 h / 0 °C

6.1: methanol; sodium tetrahydroborate / 1 h / 0 °C

With pyridine; 1H-imidazole; hydrogenchloride; methanol; dmap; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; diethylamino-sulfur trifluoride; water; sodium hydride; 4-methylmorpholine N-oxide; In methanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.tet.2012.03.023

Reference yield:

: 1009810-93-8
(3aS,4S,6R,6aR)-4-(4-methoxybenzyloxy)-6-vinyltetrahydro-3aH-spiro[cyclopenta[d][1,3]dioxole-2,1'-cyclopentane]

: 1374851-82-7
((1R,2R,3R,4S)-2-(tert-butyldiphenylsilyloxy)-3-fluoro-4-(4-methoxybenzyloxy)cyclopentyl)methanol

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogenchloride / methanol / 25 °C

2: 1H-imidazole; dmap / dichloromethane / 2 h / 0 - 20 °C

3: pyridine; diethylamino-sulfur trifluoride / dichloromethane / 12 h / 20 °C / Inert atmosphere

4: sodium periodate; osmium(VIII) oxide; water; 4-methylmorpholine N-oxide / methanol / 2 h / 0 °C

5: methanol; sodium tetrahydroborate / 1 h / 0 °C

With pyridine; 1H-imidazole; hydrogenchloride; methanol; dmap; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; diethylamino-sulfur trifluoride; water; 4-methylmorpholine N-oxide; In methanol; dichloromethane;
DOI:10.1016/j.tet.2012.03.023