2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

Base Information

Chemical Name:2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester
CAS No.:189341-30-8
Molecular Formula:C₁₉H₂₂ClNO₅S
Molecular Weight:411.906
Hs Code.:

Synonyms:2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

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Chemical Property of 2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

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Technology Process of 2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

There total 7 articles about 2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester 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: 79.0%

: 189341-28-4
4-[3-(2-chloro-benzenesulfonyloxy)-5-hydroxymethyl-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester

: 189341-30-8
2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; for 2h;
DOI:10.1016/S0960-894X(99)00617-4

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 189341-30-8
2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: aq. NaHCO₃ / diethyl ether

2.1: NaH / dimethylformamide

2.2: dimethylformamide / 3 h / 50 °C

3.1: 61 percent / LiBH₄ / tetrahydrofuran

4.1: 79 percent / 4N HCl / dioxane / 2 h

With hydrogenchloride; lithium borohydride; sodium hydride; sodium hydrogencarbonate; In tetrahydrofuran; 1,4-dioxane; diethyl ether; N,N-dimethyl-formamide; 1.1: Sulfonylation / 2.1: Metallation / 2.2: Substitution / 3.1: Reduction / 4.1: Acidolysis;
DOI:10.1016/S0960-894X(99)00617-4

Reference yield:

: 84358-13-4,174286-31-8
N-[(tert-butoxy)carbonyl]piperidine-4-carboxylic acid

: 189341-30-8
2-chloro-benzenesulfonic acid 3-hydroxymethyl-5-(piperidin-4-ylmethoxy)-phenyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 84 percent / BH₃*THF / 0 - 25 °C

2.1: 93 percent / Et₃N / CH₂Cl₂

3.1: NaH / dimethylformamide

3.2: dimethylformamide / 3 h / 50 °C

4.1: 61 percent / LiBH₄ / tetrahydrofuran

5.1: 79 percent / 4N HCl / dioxane / 2 h

With hydrogenchloride; lithium borohydride; borane-THF; sodium hydride; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; 1.1: Reduction / 2.1: Mesylation / 3.1: Metallation / 3.2: Substitution / 4.1: Reduction / 5.1: Acidolysis;
DOI:10.1016/S0960-894X(99)00617-4