HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6-nitrobenzaldehyde → 2-(2-Chloro-6-nitrophenyl)-2-((trimethylsilyl)oxy)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6-nitrobenzaldehyde | HCID 80701 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Chloro-6-nitrophenyl)-2-((trimethylsilyl)oxy)acetonitrile | HCID 131735767 | — |
Reaction Steps
To a stirred solution of 2-chloro-6-nitrobenzaldehyde (1.0 g, 5.4 mmol) in DCM (15 mL) were added TMSCN (1.0 mL, 8.1 mmol) and NMO (0.19 g, 1.6 mmol) at room temperature and stirred for 1 h. The reaction mixture was quenched with water (50 mL) and extracted with DCM (2×30 mL). The combined organic layers were washed with water (50 mL), brine (50 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure to get compound A84-1 (1.0 g, 67%) as a brown color oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365522B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-e94cf7051ba84b05aa83aeda2365200b |
| Source note | uspto-grants-2016_06 |