benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

Base Information

Chemical Name:benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate
CAS No.:1437682-82-0
Molecular Formula:C₃₀H₄₇NO₄
Molecular Weight:485.707
Hs Code.:

Synonyms:benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

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Chemical Property of benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

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Technology Process of benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

There total 6 articles about benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-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: 79.0%

: 56606-79-2
dec-1-en-3-one

: 1437682-67-1
benzyl (2S,2αR,5R)-(+)-5-allyl-2-(1-hydroxyheptyl)pyrrolidine-1-carboxylate

: 1437682-82-0
benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

Guidance literature:: With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; In dichloromethane; for 22h; Reflux;
DOI:10.1002/ejoc.201200974

Reference yield:

: 1437682-63-7
benzyl (2S,5R)-(-)-5-allyl-2-heptanoylpyrrolidine-1-carboxylate

: 1437682-82-0
benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: cerium(III) chloride heptahydrate / methanol / 0.17 h / 0 °C

1.2: 21 h / 0 - 20 °C

2.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 22 h / Reflux

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; cerium(III) chloride heptahydrate; In methanol; dichloromethane; 1.1: |Luche Cerium Reduction;
DOI:10.1002/ejoc.201200974

Reference yield:

: 123457-52-3
(2S,5R)-5-allylpyrrolidine-1,2-dicarboxylic acid 1-benzylester 2-methylester

: 1437682-82-0
benzyl (2S,2αS,5R)-2-(1-hydroxyheptyl)-5-[(E)-4-oxoundec-2-enyl]-pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: Super Hydride / tetrahydrofuran / 2 h / 0 °C

2.1: pyridinium chlorochromate / dichloromethane / 20 h / 0 - 20 °C

3.1: tetrahydrofuran / 24 h / 0 - 20 °C

4.1: pyridinium chlorochromate / dichloromethane / 23 h / 20 °C

5.1: cerium(III) chloride heptahydrate / methanol / 0.17 h / 0 °C

5.2: 21 h / 0 - 20 °C

6.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 22 h / Reflux

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; cerium(III) chloride heptahydrate; Super Hydride; pyridinium chlorochromate; In tetrahydrofuran; methanol; dichloromethane; 5.1: |Luche Cerium Reduction;
DOI:10.1002/ejoc.201200974