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

Base Information

Chemical Name:4-[3-(2-chloro-benzenesulfonyloxy)-5-hydroxymethyl-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:189341-28-4
Molecular Formula:C₂₄H₃₀ClNO₇S
Molecular Weight:512.024
Hs Code.:

4-[3-(2-chloro-benzenesulfonyloxy)-5-hydroxymethyl-phenoxymethyl]-piperidine-1-carboxylic acid <i>tert</i>-butyl ester

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

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Chemical Property of 4-[3-(2-chloro-benzenesulfonyloxy)-5-hydroxymethyl-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-[3-(2-chloro-benzenesulfonyloxy)-5-hydroxymethyl-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester

There total 7 articles about 4-[3-(2-chloro-benzenesulfonyloxy)-5-hydroxymethyl-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl 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: 61.0%

: 189340-02-1
2-Chlorobenzenesulfonic acid 3-[[1-N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]-5-carbomethoxyphenyl ester

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

Guidance literature:: With lithium borohydride; In tetrahydrofuran;
DOI:10.1016/S0960-894X(99)00617-4

Reference yield:

: 498-94-2
isonipecotic acid

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

Guidance literature:: Multi-step reaction with 5 steps

1.1: 91 percent / NaHCO₃ / dioxane; H₂O / 24 h

2.1: 84 percent / BH₃*THF / 0 - 25 °C

3.1: 93 percent / Et₃N / CH₂Cl₂

4.1: NaH / dimethylformamide

4.2: dimethylformamide / 3 h / 50 °C

5.1: 61 percent / LiBH₄ / tetrahydrofuran

With lithium borohydride; borane-THF; sodium hydride; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; 1.1: Acylation / 2.1: Reduction / 3.1: Mesylation / 4.1: Metallation / 4.2: Substitution / 5.1: Reduction;
DOI:10.1016/S0960-894X(99)00617-4

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

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

Guidance literature:: Multi-step reaction with 5 steps

1.1: 91 percent / NaHCO₃ / dioxane; H₂O / 24 h

2.1: 84 percent / BH₃*THF / 0 - 25 °C

3.1: 93 percent / Et₃N / CH₂Cl₂

4.1: NaH / dimethylformamide

4.2: dimethylformamide / 3 h / 50 °C

5.1: 61 percent / LiBH₄ / tetrahydrofuran

With lithium borohydride; borane-THF; sodium hydride; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; 1.1: Acylation / 2.1: Reduction / 3.1: Mesylation / 4.1: Metallation / 4.2: Substitution / 5.1: Reduction;
DOI:10.1016/S0960-894X(99)00617-4