2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

Base Information

Chemical Name:2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol
CAS No.:220467-08-3
Molecular Formula:C₁₈H₂₆O₂
Molecular Weight:274.403
Hs Code.:

Synonyms:2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

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Chemical Property of 2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

Chemical Property:

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Technology Process of 2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

There total 4 articles about 2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol 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:

: 99277-05-1
(1R,2R)-2-Bromomethyl-1-(2-hydroxyethyl)-2-methyl-3-methylenecyclopentane

: 220467-08-3
2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / KN(TMS)2 / tetrahydrofuran / 0 °C

2: 93 percent / 1,2-dimethoxy-ethane; hexamethylphosphoric acid triamide / 48 h / 100 °C

3: 70 percent / 1.) DIBAH; 2.) H₃O⁽¹⁺⁾ / toluene / 0.5 h / 0 °C

4: 92 percent / LiAlH₄ / diethyl ether / 0.5 h / 0 °C

With lithium aluminium tetrahydride; oxonium; potassium hexamethylsilazane; diisobutylaluminium hydride; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; 1,2-dimethoxyethane; diethyl ether; toluene;
DOI:10.1016/S0040-4039(98)02535-0

Reference yield:

: 104758-32-9
(1R,2R)-2-Bromomethyl-1-methoxycarbonylmethyl-2-methyl-3-methylenecyclopentane

: 220467-08-3
2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / LiAlH₄ / diethyl ether / 1.5 h / -60 °C

2: 93 percent / KN(TMS)2 / tetrahydrofuran / 0 °C

3: 93 percent / 1,2-dimethoxy-ethane; hexamethylphosphoric acid triamide / 48 h / 100 °C

4: 70 percent / 1.) DIBAH; 2.) H₃O⁽¹⁺⁾ / toluene / 0.5 h / 0 °C

5: 92 percent / LiAlH₄ / diethyl ether / 0.5 h / 0 °C

With lithium aluminium tetrahydride; oxonium; potassium hexamethylsilazane; diisobutylaluminium hydride; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; 1,2-dimethoxyethane; diethyl ether; toluene;
DOI:10.1016/S0040-4039(98)02535-0

Reference yield:

: 220466-90-0
[2-((1R,2R)-2-Bromomethyl-2-methyl-3-methylene-cyclopentyl)-ethoxymethyl]-benzene

: 220467-08-3
2-[(1R,2R)-2-(2-Benzyloxy-ethyl)-1-methyl-5-methylene-cyclopentyl]-ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / 1,2-dimethoxy-ethane; hexamethylphosphoric acid triamide / 48 h / 100 °C

2: 70 percent / 1.) DIBAH; 2.) H₃O⁽¹⁺⁾ / toluene / 0.5 h / 0 °C

3: 92 percent / LiAlH₄ / diethyl ether / 0.5 h / 0 °C

With lithium aluminium tetrahydride; oxonium; diisobutylaluminium hydride; In N,N,N,N,N,N-hexamethylphosphoric triamide; 1,2-dimethoxyethane; diethyl ether; toluene;
DOI:10.1016/S0040-4039(98)02535-0