{2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

Base Information

Chemical Name:{2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol
CAS No.:607708-13-4
Molecular Formula:C₂₀H₁₇Cl₂NOS
Molecular Weight:390.333
Hs Code.:

Synonyms:{2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

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Chemical Property of {2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

Chemical Property:

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Technology Process of {2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

There total 5 articles about {2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol 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: 73.0%

: 106-38-7
para-bromotoluene

: 441052-91-1
2,6-dichloro-4-[(phenylthio)methyl]nicotinaldehyde

: 607708-13-4
{2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

Guidance literature:: para-bromotoluene; With magnesium; In tetrahydrofuran;

2,6-dichloro-4-[(phenylthio)methyl]nicotinaldehyde; In tetrahydrofuran; at -78 - 0 ℃;
DOI:10.1021/jo0344081

Reference yield:

: 441052-90-0
2,6-dichloro-4-[(phenylthio)methyl]nicotinonitrile

: 607708-13-4
{2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: 62 percent / diisobutylaluminum hydride / CH₂Cl₂; toluene / -78 - 20 °C

2.1: Mg / tetrahydrofuran

2.2: 73 percent / tetrahydrofuran / -78 - 0 °C

With diisobutylaluminium hydride; magnesium; In tetrahydrofuran; dichloromethane; toluene; 2.2: Grignard reaction;
DOI:10.1021/jo0344081

Reference yield:

: 25907-38-4
ethyl 4-(phenylthio)-acetoacetate

: 607708-13-4
{2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: 55 percent / potassium hydroxide / methanol / 7 h / Heating

2.1: 54 percent / phosphorus oxychloride / 9 h / 150 °C

3.1: 62 percent / diisobutylaluminum hydride / CH₂Cl₂; toluene / -78 - 20 °C

4.1: Mg / tetrahydrofuran

4.2: 73 percent / tetrahydrofuran / -78 - 0 °C

With potassium hydroxide; diisobutylaluminium hydride; magnesium; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; toluene; 4.2: Grignard reaction;
DOI:10.1021/jo0344081