(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

Base Information

Chemical Name:(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate
CAS No.:1369492-91-0
Molecular Formula:C₂₈H₃₆O₆
Molecular Weight:468.59
Hs Code.:

Synonyms:(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

Suppliers and Price of (4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

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 (4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

There total 9 articles about (4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate 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: 88.0%

: 1369492-90-9
(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-(tertbutyldimethylsilyloxy)-4-(4-methoxybenzyloxy)oct-2-enoate

: 1369492-91-0
(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

Guidance literature:: With toluene-4-sulfonic acid; In methanol; at 0 ℃; for 0.5h;
DOI:10.1016/j.tetasy.2012.01.014

Reference yield:

: 79414-02-1,121785-58-8,121785-61-3,133522-08-4,133522-10-8,133522-11-9,133522-09-5
methyl (-)-(5R,2E)-5-(tert-butyldimethylsilyloxy)hexenoate

: 1369492-91-0
(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

Guidance literature:: Multi-step reaction with 9 steps

1.1: sodium tetrahydroborate; nickel(II) chloride hexahydrate / methanol / 1 h / 0 - 20 °C

2.1: diisobutylaluminium hydride / dichloromethane / 0.5 h / -78 °C

2.2: 0.5 h / Saturated solution

3.1: L-proline / dimethyl sulfoxide / 20 °C / Inert atmosphere

4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / dimethyl sulfoxide; acetonitrile / 1 h / 0 - 20 °C / Inert atmosphere

5.1: copper(ll) sulfate pentahydrate / methanol / 20 °C

6.1: toluene-4-sulfonic acid / dichloromethane / 8 h / 0 - 20 °C

7.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 8 h / 20 °C

8.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 12 h / 0 °C

9.1: toluene-4-sulfonic acid / methanol / 0.5 h / 0 °C

With dmap; sodium tetrahydroborate; copper(ll) sulfate pentahydrate; nickel(II) chloride hexahydrate; lithium hydroxide monohydrate; diisobutylaluminium hydride; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; dicyclohexyl-carbodiimide; L-proline; lithium chloride; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile; 4.1: Horner-Wadsworth-Emmons olefination;
DOI:10.1016/j.tetasy.2012.01.014

Reference yield:

: 110236-68-5
(2R,3S)-3-(benzyloxy)pent-4-en-2-ol

: 1369492-91-0
(4R,7R,E)-((2R,3S)-3-(benzyloxy)pent-4-en-2-yl) 7-hydroxy-4-(4-methoxybenzyloxy)oct-2-enoate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 12 h / 0 °C

2: toluene-4-sulfonic acid / methanol / 0.5 h / 0 °C

With dmap; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; In methanol; dichloromethane;
DOI:10.1016/j.tetasy.2012.01.014