1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Base Information

Chemical Name:1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene
CAS No.:467252-67-1
Molecular Formula:C₁₉H₃₁ClO₅S
Molecular Weight:406.971
Hs Code.:

Synonyms:1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Suppliers and Price of 1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

There total 6 articles about 1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene 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:

: 467252-62-6
3-{[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethyl]sulfanyl}-2-methylbenzyl alcohol

: 467252-67-1
1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Guidance literature:: With thionyl chloride; In dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1021/jm0208673

Reference yield:

: 1975-50-4
2-methyl-3-nitrobenzic acid

: 467252-67-1
1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Guidance literature:: Multi-step reaction with 6 steps

1.1: H₂ / Pd/C

2.1: NaNO₂; H⁺

2.2: potassium ethyl xanthogenate; aq. Na₂CO₃ / pH 8

2.3: 14.66 g / aq. NaOH / 20 h / Heating

3.1: 93 percent / H₂SO₄ / 48 h / Heating

4.1: 96 percent / LiAlH₄ / tetrahydrofuran / 2 h / Heating

5.1: 32 percent / Et₃N / acetonitrile / 72 h / 20 °C

6.1: SOCl₂ / CH₂Cl₂ / 0.5 h / 20 °C

With lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; hydrogen; hydrogen cation; triethylamine; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm0208673

Reference yield:

: 52130-17-3
3-amino-2-methylbenzoic acid

: 467252-67-1
1-chloromethyl-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethylsulfanyl]-2-methyl-benzene

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaNO₂; H⁺

1.2: potassium ethyl xanthogenate; aq. Na₂CO₃ / pH 8

1.3: 14.66 g / aq. NaOH / 20 h / Heating

2.1: 93 percent / H₂SO₄ / 48 h / Heating

3.1: 96 percent / LiAlH₄ / tetrahydrofuran / 2 h / Heating

4.1: 32 percent / Et₃N / acetonitrile / 72 h / 20 °C

5.1: SOCl₂ / CH₂Cl₂ / 0.5 h / 20 °C

With lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; hydrogen cation; triethylamine; sodium nitrite; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm0208673