2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole

Base Information

• Chemical Name: 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole
• CAS No.: 732283-57-7
• Molecular Formula: C₂₄H₂₀NOPS₆
• Molecular Weight: 561.799
• Mol file: 732283-57-7.mol

Synonyms:2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole

Chemical Property of 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole

There total 3 articles about 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole 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: 27.0%

(+/-)-2-(ethylenedithio-tetrathiafulvalenyl)-4-methyl-2-oxazoline (732283-41-9) + chloro-diphenylphosphine (1079-66-9,74391-44-9) → 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole (732283-57-7)

Guidance literature:

(+/-)-2-(ethylenedithio-tetrathiafulvalenyl)-4-methyl-2-oxazoline; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 4h;

chloro-diphenylphosphine; In tetrahydrofuran; at 20 ℃;

DOI:10.1039/b402877e

Reference yield:

2-(+/-)-N-(1-hydroxy-propyl)-ethylenedithio-tetrathiafulvalene-carboxamide (732283-12-4) → 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole (732283-57-7)

Guidance literature:

Multi-step reaction with 3 steps

1.1: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

2.1: tetrahydrofuran / 20 h / 50 °C

3.1: LDA / tetrahydrofuran / 4 h / -78 °C

3.2: 27 percent / tetrahydrofuran / 20 °C

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran;

DOI:10.1039/b402877e

Reference yield:

4,5-ethylenedithiotetrathiafulvalene-4'-carbonyl chloride (251901-42-5) → 2-[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5-diphenylphosphanyl-[1,3]dithiol-4-yl]-4-methyl-4,5-dihydro-oxazole (732283-57-7)

Guidance literature:

Multi-step reaction with 4 steps

1.1: Et₃N / tetrahydrofuran / 12 h / 20 °C

2.1: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

3.1: tetrahydrofuran / 20 h / 50 °C

4.1: LDA / tetrahydrofuran / 4 h / -78 °C

4.2: 27 percent / tetrahydrofuran / 20 °C

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran;

DOI:10.1039/b402877e

upstream raw materials:

(+/-)-2-(ethylenedithio-tetrathiafulvalenyl)-4-methyl-2-oxazoline

chloro-diphenylphosphine

2-(+/-)-N-(1-hydroxy-propyl)-ethylenedithio-tetrathiafulvalene-carboxamide

4,5-ethylenedithiotetrathiafulvalene-4'-carbonyl chloride