4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Base Information

Chemical Name:4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)
CAS No.:260967-78-0
Molecular Formula:C₄₃H₄₁NO₈S₂
Molecular Weight:763.932
Hs Code.:

Synonyms:4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Suppliers and Price of 4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of 4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

There total 5 articles about 4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate) 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: 86.0%

: 98-59-9
p-toluenesulfonyl chloride

: 260967-83-7
4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol

: 260967-78-0
4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Guidance literature:: With potassium hydroxide; In tetrahydrofuran; 1.) 0 deg C, 2 h, 2.) RT, 4 h;
DOI:10.1016/S0957-4166(99)00515-7

Reference yield:

: 76-83-5
trityl chloride

: 260967-78-0
4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / pyridine / 168000 h / 20 °C

2: 80 percent / K₂CO₃ / dimethylformamide / 72 h / 110 °C

3: 86 percent / KOH / tetrahydrofuran / 1.) 0 deg C, 2 h, 2.) RT, 4 h

With pyridine; potassium hydroxide; potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Alkylation / 2: Condensation / 3: Tosylation;
DOI:10.1016/S0957-4166(99)00515-7

Reference yield:

: 98828-63-8
(4-((tetrahydro-2H-pyran-2-yl)oxy)pyridine-2,6-diyl)dimethanol

: 260967-78-0
4-(3-trityloxypropyloxy)-2,6-pyridinedimethanol-bis(4-methyl-benzenesulphonate)

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / aq. AcOH / ethanol / 2 h / 120 °C

2: 80 percent / K₂CO₃ / dimethylformamide / 72 h / 110 °C

3: 86 percent / KOH / tetrahydrofuran / 1.) 0 deg C, 2 h, 2.) RT, 4 h

With potassium hydroxide; potassium carbonate; acetic acid; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; 1: detosylation / 2: Condensation / 3: Tosylation;
DOI:10.1016/S0957-4166(99)00515-7