2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

Base Information

Chemical Name:2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate
CAS No.:280762-70-1
Molecular Formula:C₂₂H₃₀ClNO₄Si
Molecular Weight:436.023
Hs Code.:

Synonyms:2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

Suppliers and Price of 2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

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 2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

There total 13 articles about 2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate 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: 63.0%

: 3-[3-benzyloxy-4-chloromethyl-5-(4-methoxy-benzyloxymethyl)-pyridin-2-yl]-propionic acid 2-trimethylsilanyl-ethyl ester

: 280762-70-1
2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; water; at 20 ℃; for 0.75h;
DOI:10.1016/S0040-4020(00)00121-6

Reference yield:

: 1136-52-3
(2,2,8-trimethyl-4H-[1,3]dioxino[4,5-c]pyridin-5-yl)methanol

: 280762-70-1
2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

Guidance literature:: Multi-step reaction with 10 steps

1: 95 percent / NaH / dimethylformamide / 15 h / 20 °C

2: m-CPBA / CHCl₃ / 2 h / 20 °C

3: 26.8 g / trifluoroacetic anhydride / CH₂Cl₂ / 5 h / 20 °C

4: 89 percent / MnO₂ / CHCl₃ / 21 h / 20 °C

5: CH₂Cl₂ / 1.5 h / 20 °C

6: H₂ / Pd/C / methanol / 0.58 h / 775.72 Torr

7: 41 percent / pyridinium p-toluenesulfonate / ethanol / 28 h / Heating

8: 88 percent / NaOEt / xylene / 5 h / Heating

9: 95 percent / SOCl₂ / benzene / 0.02 h / Heating

10: 63 percent / DDQ / CH₂Cl₂; H₂O / 0.75 h / 20 °C

With manganese(IV) oxide; thionyl chloride; hydrogen; sodium ethanolate; pyridinium p-toluenesulfonate; sodium hydride; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic anhydride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In methanol; ethanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; xylene; benzene; 1: Etherification / 2: Oxidation / 3: Rearrangement / 4: Oxidation / 5: Wittig reaction / 6: Catalytic hydrogenation / 7: Hydrolysis / 8: Substitution / 9: Substitution / 10: Hydrolysis;
DOI:10.1016/S0040-4020(00)00121-6

Reference yield:

: 2916-68-9
2-(Trimethylsilyl)ethanol

: 280762-70-1
2-(trimethylsilyl) ethyl-3-[3-(benzyloxy)-4-(chloromethyl)-5-(hydroxymethyl)-2-pyridinyl]propanoate

Guidance literature:: Multi-step reaction with 8 steps

1.1: 96 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

2.1: benzene / 18 h / Heating

2.2: 70 percent / KOH / CH₂Cl₂; H₂O

3.1: CH₂Cl₂ / 1.5 h / 20 °C

4.1: H₂ / Pd/C / methanol / 0.58 h / 775.72 Torr

5.1: 41 percent / pyridinium p-toluenesulfonate / ethanol / 28 h / Heating

6.1: 88 percent / NaOEt / xylene / 5 h / Heating

7.1: 95 percent / SOCl₂ / benzene / 0.02 h / Heating

8.1: 63 percent / DDQ / CH₂Cl₂; H₂O / 0.75 h / 20 °C

With pyridine; thionyl chloride; hydrogen; sodium ethanolate; pyridinium p-toluenesulfonate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium on activated charcoal; In methanol; ethanol; dichloromethane; water; xylene; benzene; 1.1: Esterification / 2.1: Condensation / 2.2: Hydrolysis / 3.1: Wittig reaction / 4.1: Catalytic hydrogenation / 5.1: Hydrolysis / 6.1: Substitution / 7.1: Substitution / 8.1: Hydrolysis;
DOI:10.1016/S0040-4020(00)00121-6