Technology Process of 8-bromo-3-methoxy-6,7-dihydro-5H-benzo[7]annulen-9-yl acetate
There total 6 articles about 8-bromo-3-methoxy-6,7-dihydro-5H-benzo[7]annulen-9-yl acetate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
6-bromo-2-methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-one;
With
lithium hexamethyldisilazane;
In
tetrahydrofuran;
at -70 ℃;
for 0.25h;
Inert atmosphere;
acetic anhydride;
In
tetrahydrofuran;
at 20 ℃;
for 20h;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: potassium tert-butylate / methanol / 5 h / Reflux
2.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 2 h / 20 °C / 2585.81 Torr
3.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 15 h / -5 - 20 °C
3.2: pH 2 - 3
4.1: PPA / chlorobenzene / 15 h / 80 °C
5.1: bromine / diethyl ether / 2 h
6.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.25 h / -78 °C
6.2: 0.5 h / -78 - 0 °C
With
lithium hydroxide monohydrate; potassium tert-butylate; water; hydrogen; bromine; lithium hexamethyldisilazane;
palladium 10% on activated carbon;
In
tetrahydrofuran; methanol; diethyl ether; chlorobenzene;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 2 h / 20 °C / 2585.81 Torr
2.1: water; lithium hydroxide monohydrate / tetrahydrofuran; methanol / 15 h / -5 - 20 °C
2.2: pH 2 - 3
3.1: PPA / chlorobenzene / 15 h / 80 °C
4.1: bromine / diethyl ether / 2 h
5.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.25 h / -78 °C
5.2: 0.5 h / -78 - 0 °C
With
lithium hydroxide monohydrate; water; hydrogen; bromine; lithium hexamethyldisilazane;
palladium 10% on activated carbon;
In
tetrahydrofuran; methanol; diethyl ether; chlorobenzene;