methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

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Chemical Name:methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate
CAS No.:1232828-90-8
Molecular Formula:C₂₇H₃₄FNO₄
Molecular Weight:455.57
Hs Code.:

Synonyms:methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

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Chemical Property of methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

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Technology Process of methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

There total 7 articles about methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate 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: 61.0%

: 1232828-91-9
methyl (2E)-3-(2-{(1R)-1-[(2R)-oxiran-2-yl methoxy]ethyl}phenyl)prop-2-enoate

: 1232828-89-5
(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidine

: 1232828-90-8
methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

Guidance literature:: With lithium perchlorate; In toluene; at 20 ℃; for 16h;

Reference yield:

: 185077-02-5
(3-fluoro-4-methylphenyl)magnesium bromide

: 1232828-90-8
methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

Guidance literature:: Multi-step reaction with 6 steps

1: tetrahydrofuran / 16 h / 20 °C / Inert atmosphere; Cooling with ice

2: sodium tetrahydroborate; methanol / 0.5 h / 20 °C / Cooling with ice

3: dmap / tetrahydrofuran / 16 h / Reflux

4: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 6 h / Reflux

5: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

6: lithium perchlorate / toluene / 16 h / 20 °C

With methanol; dmap; sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; lithium perchlorate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene;

Reference yield:

: 1232828-85-1
tert-butyl (2S)-2-(3-fluoro-4-methylbenzoyl)pyrrolidine-1-carboxylate

: 1232828-90-8
methyl (2E)-3-{2-[(1R)-1-({(2R)-3-[(2S)-2-(3-fluoro-4-methylbenzyl)pyrrolidin-1-yl]-2-hydroxypropyl}oxy)ethyl]phenyl}prop-2-enoate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium tetrahydroborate; methanol / 0.5 h / 20 °C / Cooling with ice

2: dmap / tetrahydrofuran / 16 h / Reflux

3: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 6 h / Reflux

4: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

5: lithium perchlorate / toluene / 16 h / 20 °C

With methanol; dmap; sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; lithium perchlorate; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene;