(1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

Base Information

Chemical Name:(1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan
CAS No.:126664-43-5
Molecular Formula:C₁₉H₂₈O₂
Molecular Weight:288.43
Hs Code.:

Synonyms:(1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

Suppliers and Price of (1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

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

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Chemical Property of (1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

Chemical Property:

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Technology Process of (1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

There total 3 articles about (1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan 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:

: 108391-93-1
(1S,6R,9R)-9-(Benzyloxy)-3-oxabicyclo<4.3.0>nonan-2-ol

: 126664-43-5
(1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

Guidance literature:: Multi-step reaction with 3 steps

1: K-hexamethyldisilazide / 1.) THF, toluene, 20 min, RT, 2.) a) - 78 deg C, 1 h, b) RT, 1 h

2: 70 percent HClO₄ / diethyl ether / 0.67 h / - 30 deg C to RT

3: K-hexamethyldisilazide / 1.) THF, toluene, 20 min, RT, 2.) a) -78 deg C, b) RT, 30 min

With perchloric acid; K-hexamethyldisilazide; In diethyl ether;

Reference yield:

: 126664-42-4,126783-81-1
(1R,2R,3R)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-methoxyethenyl)cyclopentan

: 126664-43-5
(1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent HClO₄ / diethyl ether / 0.67 h / - 30 deg C to RT

2: K-hexamethyldisilazide / 1.) THF, toluene, 20 min, RT, 2.) a) -78 deg C, b) RT, 30 min

With perchloric acid; K-hexamethyldisilazide; In diethyl ether;

Reference yield:

: 16721-43-0
n-propyltriphenylphosphonium chloride

: [(1S,2R,5R)-2-Benzyloxy-5-(2-hydroxy-ethyl)-cyclopentyl]-acetaldehyde

: 126664-43-5
(1R,2S,3R,2''Z)-3-(Benzyloxy)-1-(2-hydroxyethyl)-2-(2-pentenyl)cyclopentan

Guidance literature:: With K-hexamethyldisilazide; Yield given. Multistep reaction; 1.) THF, toluene, 20 min, RT, 2.) a) -78 deg C, b) RT, 30 min;