4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1417718-35-4
Molecular Formula:C₂₅H₃₃NO₅S
Molecular Weight:459.607
Hs Code.:

Synonyms:4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

There total 4 articles about 4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-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: 90.0%

: 87660-09-1
4-(2,4,6-trimethyl-benzenesulfonyl)-phenol

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1417718-35-4
4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 25 ℃; for 16h; Inert atmosphere;
DOI:10.1021/jm3014162

Reference yield:

: 84113-59-7
2-(4-methoxy-benzenesulfonyl)-1,3,5-trimethyl-benzene

: 1417718-35-4
4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: boron tribromide / dichloromethane / 16 h / 0 - 25 °C / Inert atmosphere

2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 16 h / 25 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; boron tribromide; triphenylphosphine; In tetrahydrofuran; dichloromethane; 2: |Mitsunobu Displacement;
DOI:10.1021/jm3014162

Reference yield:

: 108-67-8
1,3,5-trimethyl-benzene

: 1417718-35-4
4-[4-(2,4,6-trimethyl-benzenesulfonyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: aluminum (III) chloride / dichloromethane / 2 h / 25 °C / Inert atmosphere

2: boron tribromide / dichloromethane / 16 h / 0 - 25 °C / Inert atmosphere

3: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 16 h / 25 °C / Inert atmosphere

With aluminum (III) chloride; di-isopropyl azodicarboxylate; boron tribromide; triphenylphosphine; In tetrahydrofuran; dichloromethane; 3: |Mitsunobu Displacement;
DOI:10.1021/jm3014162