HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(((tert-Butyldimethylsilyl)oxy)methyl)picolinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromo-3-((tert-butyldimethylsilyloxy)methyl)pyridine | HCID 22725093 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 3-(((tert-Butyldimethylsilyl)oxy)methyl)picolinonitrile | HCID 23092627 | 82% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 2-bromo-3-((tert-butyldimethylsilyloxy)methyl)pyridine (30.1 g, 100.0 mmol, 1 eq.) and Zn(CN)2 (23.5 g, 200.0 mmol, 2.0 eq.) in DMF (100.0 mL) was purged with N2 for 5 min and added Pd(PPh3)4 (5.78 g, 5.0 mmol, 0.05 eq.). The mixture was heated at 120° C. for 2 h under N2, cooled, filtered, concentrated, and purified on silica gel using a mixture of EtOAc and hexanes as eluent to give 3-((tert-butyldimethylsilyloxy)methyl)picolinonitrile (20.4 g, 82%) as a colorless oil. LRMS (M+H+) m/z 249.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012450B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-1c431e1de2c042b493adabce4c89d5c2 |
| Source note | uspto-grants-2015_04 |