(1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

Base Information

Chemical Name:(1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate
CAS No.:339148-71-9
Molecular Formula:C₂₂H₃₂O₅
Molecular Weight:376.493
Hs Code.:

Synonyms:(1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

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Chemical Property of (1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

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Technology Process of (1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

There total 6 articles about (1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate 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: 59.0%

: 61586-79-6
ethyl (1R,2S)-2-hydroxycyclopentanecarboxylate

: 339148-63-9
(Z)-6-iodo-1-(4-methoxyphenyl)methoxy-2-hexene

: 339148-71-9
(1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide; In tetrahydrofuran; hexane; at -45 ℃; for 1h;

Reference yield:

: 1002-37-5
6-chloro-2-hexyn-1-ol

: 339148-71-9
(1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / NaH; nBu₄NI / tetrahydrofuran / 5 h / 0 - 20 °C

2: 89 percent / H₂; quinoline / Lindlar catalyst / hexane / 20 h / 20 °C / 760 Torr

3: 90 percent / NaI / acetone / 26 h / Heating

4: 59 percent / LDA; HMPA / hexane; tetrahydrofuran / 1 h / -45 °C

With quinoline; N,N,N,N,N,N-hexamethylphosphoric triamide; hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium iodide; lithium diisopropyl amide; Lindlar's catalyst; In tetrahydrofuran; hexane; acetone;

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 339148-71-9
(1R,2S,Z)-ethyl 2-hydroxy-1-[6-(4-methoxyphenylmethoxy)-4-hexenyl]cyclopentane-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / NaH; nBu₄NI / tetrahydrofuran / 5 h / 0 - 20 °C

2: 89 percent / H₂; quinoline / Lindlar catalyst / hexane / 20 h / 20 °C / 760 Torr

3: 90 percent / NaI / acetone / 26 h / Heating

4: 59 percent / LDA; HMPA / hexane; tetrahydrofuran / 1 h / -45 °C

With quinoline; N,N,N,N,N,N-hexamethylphosphoric triamide; hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium iodide; lithium diisopropyl amide; Lindlar's catalyst; In tetrahydrofuran; hexane; acetone;