Technology Process of [7,7-2H2]-1-bromoundecane
There total 10 articles about [7,7-2H2]-1-bromoundecane which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
N-Bromosuccinimide;
In
N,N-dimethyl-formamide;
at 50 ℃;
for 0.25h;
DOI:10.1021/jo010560w
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 81 percent / n-BuLi / tetrahydrofuran / 1 h / -78 °C
2: 85 percent / N-bromosuccinimide / acetone; H2O / 0.08 h / -20 °C
3: 92 percent / NaBD4 / methanol / 1 h / 20 °C
4: 73 percent / trimethylamine hydrochloride; triethylamine / CH2Cl2 / 1.5 h / 0 °C
5: LiAlD4 / diethyl ether / 3 h / 20 °C
6: 0.286 g / HCl / methanol / 16 h / 20 °C
7: 74 percent / N-bromosuccinimide / dimethylformamide / 0.25 h / 50 °C
With
hydrogenchloride; N-Bromosuccinimide; n-butyllithium; lithium aluminium deuteride; sodium borodeuteride; trimethylamine hydrochloride; triethylamine;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jo010560w
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 93 percent / BF3*OEt2; acetic acid / CHCl3 / 16 h / Heating
2: 81 percent / n-BuLi / tetrahydrofuran / 1 h / -78 °C
3: 85 percent / N-bromosuccinimide / acetone; H2O / 0.08 h / -20 °C
4: 92 percent / NaBD4 / methanol / 1 h / 20 °C
5: 73 percent / trimethylamine hydrochloride; triethylamine / CH2Cl2 / 1.5 h / 0 °C
6: LiAlD4 / diethyl ether / 3 h / 20 °C
7: 0.286 g / HCl / methanol / 16 h / 20 °C
8: 74 percent / N-bromosuccinimide / dimethylformamide / 0.25 h / 50 °C
With
hydrogenchloride; N-Bromosuccinimide; n-butyllithium; lithium aluminium deuteride; sodium borodeuteride; boron trifluoride diethyl etherate; trimethylamine hydrochloride; acetic acid; triethylamine;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; chloroform; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jo010560w