2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine

Base Information

• Chemical Name: 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine
• CAS No.: 220312-31-2
• Molecular Formula: C₂₈H₂₉NO₂S₂
• Molecular Weight: 475.676
• Mol file: 220312-31-2.mol

Synonyms:2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine

Chemical Property of 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine

There total 3 articles about 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine 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: 81.0%

diphenyldisulfane (882-33-7) + 2-(4-Methoxy-phenyl)-1-[2-((E)-3-phenylsulfanyl-allyl)-pyrrolidin-1-yl]-ethanone (220312-30-1) → 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine (220312-31-2)

Guidance literature:

With lithium diisopropyl amide; In tetrahydrofuran;

DOI:10.3987/COM-98-S(H)13

Reference yield:

2-((E)-3-Phenylsulfanyl-allyl)-pyrrolidine → 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine (220312-31-2)

Guidance literature:

Multi-step reaction with 2 steps

1.1: Me₃SiI / acetonitrile

1.2: 57 percent / Et₃N / CH₂Cl₂

2.1: 81 percent / LDA / tetrahydrofuran

With trimethylsilyl iodide; lithium diisopropyl amide; In tetrahydrofuran; acetonitrile; 1.1: Decarbonylation / 1.2: Acylation / 2.1: Thioetherification;

DOI:10.3987/COM-98-S(H)13

Reference yield:

4-methoxyphenyl-acetic chloride (4693-91-8) → 2-[3-(phenylthio)prop-2-enyl]-N-[α-(p-methoxyphenyl)-α-(phenylthio)acetyl]pyrrolidine (220312-31-2)

Guidance literature:

Multi-step reaction with 2 steps

1.1: Me₃SiI / acetonitrile

1.2: 57 percent / Et₃N / CH₂Cl₂

2.1: 81 percent / LDA / tetrahydrofuran

With trimethylsilyl iodide; lithium diisopropyl amide; In tetrahydrofuran; acetonitrile; 1.1: Decarbonylation / 1.2: Acylation / 2.1: Thioetherification;

DOI:10.3987/COM-98-S(H)13

upstream raw materials:

diphenyldisulfane

2-(4-Methoxy-phenyl)-1-[2-((E)-3-phenylsulfanyl-allyl)-pyrrolidin-1-yl]-ethanone

4-methoxyphenyl-acetic chloride

Downstream raw materials:

6-(4-methoxy-phenyl)-7-phenylsulfanylmethyl-hexahydro-indolizin-5-one

4-[7-methyl-1,2,3,5,8,8a-hexahydroindolizin-6-yl]phenol

6-(4-methoxyphenyl)-7-methyl-1,2,3,5,8,8a-hexahydroindolizine

6-(4-methoxyphenyl)-7-methyl-2,3,8,8a-tetrahydroindolizin-5(1H)-one