6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

Base Information

Chemical Name:6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester
CAS No.:1447810-98-1
Molecular Formula:C₂₉H₄₇BINO₆S
Molecular Weight:675.477
Hs Code.:

Synonyms:6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

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Chemical Property of 6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

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Technology Process of 6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

There total 7 articles about 6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl 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: 36.0%

: 1094668-77-5
6-(4-iodobenzenesulfonamido)hexanoic acid

: 1447810-92-5
(E)-11-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)undec-10-en-1-ol

: 1447810-98-1
6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

Guidance literature:: With dmap; diisopropyl-carbodiimide; In dichloromethane; at 0 ℃; for 12h;
DOI:10.1039/c3ob41020j

Reference yield:

: 132260-32-3
tert-butyldimethyl(undec-10-yn-1-yloxy)silane

: 1447810-98-1
6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetrahydrofuran / 6 h / 75 °C

1.2: 1 h / 20 °C

2.1: dmap; diisopropyl-carbodiimide / dichloromethane / 12 h / 0 °C

With dmap; diisopropyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/c3ob41020j

Reference yield:

: 2774-84-7
undec-10-yn-1-ol

: 1447810-98-1
6-(4-iodobenzenesulfonamido)hexanoic acid 11(E)-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)undec-10-enyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; dmap / dichloromethane / 26 h / 0 - 20 °C

2.1: tetrahydrofuran / 6 h / 75 °C

2.2: 1 h / 20 °C

3.1: dmap; diisopropyl-carbodiimide / dichloromethane / 12 h / 0 °C

With dmap; triethylamine; diisopropyl-carbodiimide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/c3ob41020j