1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester

Base Information

• Chemical Name: 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester
• CAS No.: 1027739-54-3
• Molecular Formula: C₂₄H₂₇NO₅S
• Molecular Weight: 441.548
• Mol file: 1027739-54-3.mol

Synonyms:1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester

Chemical Property of 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester

There total 3 articles about 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl 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:

(4-Hydroxy-phenylsulfanyl)-acetic acid ethyl ester (30519-00-7) → 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester (1027739-54-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 96 percent / K₂CO₃ / acetone / 8 h / Heating

2: aq. oxone / methanol; tetrahydrofuran / 20 °C

3: K₂CO₃; 18-crown-6; tetrabutylammonium bromide / acetone / Heating

With Oxone; 18-crown-6 ether; tetrabutylammomium bromide; potassium carbonate; In tetrahydrofuran; methanol; acetone;

DOI:10.1021/jm040086x

Reference yield:

(4-prop-2-ynyloxyphenylsulfanyl)acetic acid ethyl ester (287201-85-8) → 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester (1027739-54-3)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. oxone / methanol; tetrahydrofuran / 20 °C

2: K₂CO₃; 18-crown-6; tetrabutylammonium bromide / acetone / Heating

With Oxone; 18-crown-6 ether; tetrabutylammomium bromide; potassium carbonate; In tetrahydrofuran; methanol; acetone;

DOI:10.1021/jm040086x

Reference yield:

N,N-bis(2-chloro-ethyl)-benzenemethanamine (55-51-6) + (4-prop-2-ynyloxybenzenesulfonyl)acetic acid ethyl ester (287201-86-9) → 1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester (1027739-54-3)

Guidance literature:

With 18-crown-6 ether; tetrabutylammomium bromide; potassium carbonate; In acetone; Heating;

DOI:10.1021/jm040086x

upstream raw materials:

N,N-bis(2-chloro-ethyl)-benzenemethanamine

(4-prop-2-ynyloxybenzenesulfonyl)acetic acid ethyl ester

(4-Hydroxy-phenylsulfanyl)-acetic acid ethyl ester

(4-prop-2-ynyloxyphenylsulfanyl)acetic acid ethyl ester

Downstream raw materials:

1-benzyl-4-(4-prop-2-ynyloxy-benzenesulfonyl)-piperidine-4-carboxylic acid