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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202667Generated: November 1, 2026

2-Chloro-6-nitrobenzaldehyde → 2-(2-Chloro-6-nitrophenyl)-2-((trimethylsilyl)oxy)acetonitrile

https://huagongshe.com/reaction/2202667

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-nitrobenzaldehydeHCID 80701—
ReactantMethyl morpholine oxideHCID 82029—
ReactantTrimethylsilyl cyanideHCID 82115—
SolventDichloromethaneHCID 6344—
Product2-(2-Chloro-6-nitrophenyl)-2-((trimethylsilyl)oxy)acetonitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365522B2
Source datasetuspto-grants-2016_06
ORD IDord-e94cf7051ba84b05aa83aeda2365200b
Source noteuspto-grants-2016_06