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5-Heptenoic acid, 7-[(2R)-2-[(1E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl]-1-butenyl]-5- oxo-1-pyrrolidinyl]-, (5Z)-

Base Information
  • Chemical Name:5-Heptenoic acid, 7-[(2R)-2-[(1E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl]-1-butenyl]-5- oxo-1-pyrrolidinyl]-, (5Z)-
  • CAS No.:494222-00-3
  • Molecular Formula:C23H31NO5
  • Molecular Weight:401.503
  • Hs Code.:
5-Heptenoic acid,
7-[(2R)-2-[(1E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl]-1-butenyl]-5-
oxo-1-pyrrolidinyl]-, (5Z)-

Synonyms:

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Chemical Property of 5-Heptenoic acid, 7-[(2R)-2-[(1E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl]-1-butenyl]-5- oxo-1-pyrrolidinyl]-, (5Z)-
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Technology Process of 5-Heptenoic acid, 7-[(2R)-2-[(1E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl]-1-butenyl]-5- oxo-1-pyrrolidinyl]-, (5Z)-

There total 11 articles about 5-Heptenoic acid, 7-[(2R)-2-[(1E,3S)-3-hydroxy-4-[3-(methoxymethyl)phenyl]-1-butenyl]-5- oxo-1-pyrrolidinyl]-, (5Z)- 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:
Guidance literature:
With water; sodium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; at 20 ℃;
DOI:10.1248/cpb.59.1494
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 1.5 h / 0 - 20 °C / Inert atmosphere
1.2: 1 h / 0 °C / Inert atmosphere
2.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran; toluene / 20 °C / Inert atmosphere
3.1: water; sodium hydroxide / tetrahydrofuran; 1,2-dimethoxyethane; ethanol / 20 °C
With borane-THF; water; sodium hydride; sodium hydroxide; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; toluene; mineral oil; 1.1: Horner-Wadsworth-Emmons olefination / 1.2: Horner-Wadsworth-Emmons olefination;
DOI:10.1248/cpb.59.1494
Guidance literature:
Multi-step reaction with 5 steps
1.1: toluene-4-sulfonic acid / methanol / 4 h / 20 °C
2.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere
3.1: sodium hydride / tetrahydrofuran; mineral oil / 1.5 h / 0 - 20 °C / Inert atmosphere
3.2: 1 h / 0 °C / Inert atmosphere
4.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran; toluene / 20 °C / Inert atmosphere
5.1: water; sodium hydroxide / tetrahydrofuran; 1,2-dimethoxyethane; ethanol / 20 °C
With borane-THF; water; sulfur trioxide pyridine complex; sodium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; sodium hydroxide; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; toluene; mineral oil; 3.1: Horner-Wadsworth-Emmons olefination / 3.2: Horner-Wadsworth-Emmons olefination;
DOI:10.1248/cpb.59.1494
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