(1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

Base Information

Chemical Name:(1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene
CAS No.:1425377-62-3
Molecular Formula:C₃₁H₃₀O₃
Molecular Weight:450.577
Hs Code.:

Synonyms:(1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

Suppliers and Price of (1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

Supply Marketing:

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

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Chemical Property of (1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Hazard Codes:

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Technology Process of (1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

There total 18 articles about (1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene 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: 70.0%

: 1425377-60-1
(1R,2R,3R,4R)-4-(benzyloxy)-2-((benzyloxy)methyl)-3-((2-naphthylmethyl)oxy)cyclopentyl methanesulfonate

: 1425377-62-3
(1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

: 1425377-63-4
(1R,2R)-1-(benzyloxy)-2-((2-naphthylmethyl)oxy)-3-((benzyloxy)methyl)cyclopent-3-ene

Guidance literature:: (1R,2R,3R,4R)-4-(benzyloxy)-2-((benzyloxy)methyl)-3-((2-naphthylmethyl)oxy)cyclopentyl methanesulfonate; With sodium hydride; In methanol; N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 2.5h; Inert atmosphere;

With hydrogenchloride; In methanol; water; N,N-dimethyl-formamide; mineral oil; Inert atmosphere; Cooling with ice;
DOI:10.1002/chem.201202374

Reference yield: 55.0%

: 1425377-60-1
(1R,2R,3R,4R)-4-(benzyloxy)-2-((benzyloxy)methyl)-3-((2-naphthylmethyl)oxy)cyclopentyl methanesulfonate

: 1425377-62-3
(1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

: 1425377-63-4
(1R,2R)-1-(benzyloxy)-2-((2-naphthylmethyl)oxy)-3-((benzyloxy)methyl)cyclopent-3-ene

: 1425377-64-5
(1R,2R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-methylenecyclopent-3-ene

Guidance literature:: (1R,2R,3R,4R)-4-(benzyloxy)-2-((benzyloxy)methyl)-3-((2-naphthylmethyl)oxy)cyclopentyl methanesulfonate; With potassium tert-butylate; In N,N-dimethyl-formamide; at 100 ℃; for 0.75h; Inert atmosphere;

With hydrogenchloride; In water; N,N-dimethyl-formamide; pH=2; Reagent/catalyst; Temperature; Inert atmosphere;
DOI:10.1002/chem.201202374

Reference yield:

: 39939-07-6
5-(benzyloxymethyl)cyclopentadiene

: 1425377-62-3
(1R,2R,5R)-2-(benzyloxy)-1-((2-naphthylmethyl)oxy)-5-((benzyloxy)methyl)cyclopent-3-ene

: 1425377-63-4
(1R,2R)-1-(benzyloxy)-2-((2-naphthylmethyl)oxy)-3-((benzyloxy)methyl)cyclopent-3-ene

Guidance literature:: Multi-step reaction with 6 steps

1.1: L-diisopinocampheylborane / tetrahydrofuran / 72 h / -78 - -10 °C / Inert atmosphere

1.2: 24 h / 20 °C / Inert atmosphere

2.1: 3-chloro-benzenecarboperoxoic acid / water; dichloromethane / 6 h / 0 - 20 °C / Inert atmosphere

3.1: triethylamine / tetrahydrofuran / 5 h / 0 - 20 °C / Inert atmosphere

4.1: boron trifluoride diethyl etherate / dichloromethane / 3 h / 20 °C / Inert atmosphere

5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 18 h / 0 - 20 °C / Inert atmosphere

6.1: sodium hydride / methanol; N,N-dimethyl-formamide; mineral oil / 2.5 h / 20 °C / Inert atmosphere

6.2: Inert atmosphere; Cooling with ice

With boron trifluoride diethyl etherate; sodium hydride; triethylamine; 3-chloro-benzenecarboperoxoic acid; L-diisopinocampheylborane; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1002/chem.201202374