Technology Process of C27H51BO4Si
There total 10 articles about C27H51BO4Si which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: Et3N / diethyl ether / 2 h / 0 °C
2.1: diethyl ether / 23 h / -78 - -20 °C
3.1: lithium borohydride / diethyl ether; tetrahydrofuran / 3 h / -78 °C
3.2: 30percent aq. H2O2; 10percent aq. NaOH / methanol / 0 - 20 °C
4.1: 99 percent / 2,6-lutidine / CH2Cl2 / 2 h / -78 °C
5.1: 69 percent / CSA / methanol; CH2Cl2 / 8 h / 0 °C
6.1: 100 percent / H2 / Pd(OH)2/C / ethanol / 16 h / 20 °C
7.1: oxalyl chloride; dimethyl sulfoxide / CH2Cl2 / 2 h / -78 - -50 °C
8.1: sodium chlorite; sodium dihydrogen orthophosphate; 2-methyl-2-butene / 2-methyl-propan-2-ol; H2O / 2 h / 20 °C
9.1: diethyl ether / 20 °C
10.1: Et3N / diethyl ether / 1 h / 0 °C
With
2,6-dimethylpyridine; sodium chlorite; sodium dihydrogenphosphate; lithium borohydride; 2-methyl-but-2-ene; oxalyl dichloride; camphor-10-sulfonic acid; hydrogen; dimethyl sulfoxide; triethylamine;
palladium dihydroxide;
In
tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; water; tert-butyl alcohol;
7.1: Swern oxidation;
DOI:10.1021/ja011211m
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 99 percent / 2,6-lutidine / CH2Cl2 / 2 h / -78 °C
2: 69 percent / CSA / methanol; CH2Cl2 / 8 h / 0 °C
3: 100 percent / H2 / Pd(OH)2/C / ethanol / 16 h / 20 °C
4: oxalyl chloride; dimethyl sulfoxide / CH2Cl2 / 2 h / -78 - -50 °C
5: sodium chlorite; sodium dihydrogen orthophosphate; 2-methyl-2-butene / 2-methyl-propan-2-ol; H2O / 2 h / 20 °C
6: diethyl ether / 20 °C
7: Et3N / diethyl ether / 1 h / 0 °C
With
2,6-dimethylpyridine; sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; oxalyl dichloride; camphor-10-sulfonic acid; hydrogen; dimethyl sulfoxide; triethylamine;
palladium dihydroxide;
In
methanol; diethyl ether; ethanol; dichloromethane; water; tert-butyl alcohol;
4: Swern oxidation;
DOI:10.1021/ja011211m
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: diethyl ether / 23 h / -78 - -20 °C
2.1: lithium borohydride / diethyl ether; tetrahydrofuran / 3 h / -78 °C
2.2: 30percent aq. H2O2; 10percent aq. NaOH / methanol / 0 - 20 °C
3.1: 99 percent / 2,6-lutidine / CH2Cl2 / 2 h / -78 °C
4.1: 69 percent / CSA / methanol; CH2Cl2 / 8 h / 0 °C
5.1: 100 percent / H2 / Pd(OH)2/C / ethanol / 16 h / 20 °C
6.1: oxalyl chloride; dimethyl sulfoxide / CH2Cl2 / 2 h / -78 - -50 °C
7.1: sodium chlorite; sodium dihydrogen orthophosphate; 2-methyl-2-butene / 2-methyl-propan-2-ol; H2O / 2 h / 20 °C
8.1: diethyl ether / 20 °C
9.1: Et3N / diethyl ether / 1 h / 0 °C
With
2,6-dimethylpyridine; sodium chlorite; sodium dihydrogenphosphate; lithium borohydride; 2-methyl-but-2-ene; oxalyl dichloride; camphor-10-sulfonic acid; hydrogen; dimethyl sulfoxide; triethylamine;
palladium dihydroxide;
In
tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; water; tert-butyl alcohol;
6.1: Swern oxidation;
DOI:10.1021/ja011211m