Technology Process of 4-(2-chloro-5-isobutoxy-N-methylbenzamido)-3,5-dimethylbenzoic acid
There total 8 articles about 4-(2-chloro-5-isobutoxy-N-methylbenzamido)-3,5-dimethylbenzoic acid which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: thionyl chloride / 18 h / 60 °C
2: palladium 10% on activated carbon; hydrogen / ethyl acetate; ethanol / 20 °C
3: potassium carbonate / tetrahydrofuran / 0 - 20 °C
4: sodium hydroxide; water / tetrahydrofuran / 80 °C
5: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C
With
thionyl chloride; palladium 10% on activated carbon; water; hydrogen; sodium hydride; potassium carbonate; sodium hydroxide;
In
tetrahydrofuran; ethanol; ethyl acetate; mineral oil;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: sodium hydroxide; water / tetrahydrofuran / 80 °C
2: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C
With
water; sodium hydride; sodium hydroxide;
In
tetrahydrofuran; mineral oil;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: caesium carbonate / acetonitrile / Reflux
2: sodium hydroxide; water / methanol / 4 h / Reflux
3: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 20 °C
4: potassium carbonate / tetrahydrofuran / 0 - 20 °C
5: sodium hydroxide; water / tetrahydrofuran / 80 °C
6: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C
With
oxalyl dichloride; water; sodium hydride; potassium carbonate; caesium carbonate; N,N-dimethyl-formamide; sodium hydroxide;
In
tetrahydrofuran; methanol; acetonitrile; mineral oil;