2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

Base Information

Chemical Name:2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione
CAS No.:1237512-74-1
Molecular Formula:C₁₉H₁₇Br₂NO₃
Molecular Weight:467.157
Hs Code.:

Synonyms:2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

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Chemical Property of 2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

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Technology Process of 2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

There total 3 articles about 2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione 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: 43.0%

: (RS)-2-[2-(2,6-dimethylphenoxy)-1-methylethyl]-1H-isoindole-1,3(2H)-dione

: 1237512-74-1
2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

Guidance literature:: With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 72h; Reflux;
DOI:10.1002/ardp.200900218

Reference yield:

: 85-44-9
phthalic anhydride

: 1237512-74-1
2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / toluene / 130 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C

3: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 72 h / Reflux

With N-Bromosuccinimide; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; toluene; 2: Mitsunobu reaction;
DOI:10.1002/ardp.200900218

Reference yield:

: 211501-36-9
2-(2-hydroxy-1-methylethyl)-1H-isoindole-1,3(2H)-dione

: 1237512-74-1
2-{2-[2,6-bis(bromomethyl)phenoxy]-1-methylethyl}-1H-isoindole-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 2 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C

2: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 72 h / Reflux

With N-Bromosuccinimide; di-isopropyl azodicarboxylate; triphenylphosphine; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; 1: Mitsunobu reaction;
DOI:10.1002/ardp.200900218