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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294205Generated: October 30, 2026

N-Hydroxy-1,1,1-trimethylsilanamine → HCID 54681154, compound

https://huagongshe.com/reaction/2294205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Hydroxy-1,1,1-trimethylsilanamineHCID 21936899—
ReactantEthyl 4-hydroxy-7-nitro-2-oxo-1,2-dihydro-quinoline-3-carboxylateHCID 54681153—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54681154HCID 5468115465%

Reaction Conditions

Temperature100 °C

Reaction Steps

4 ml of trimethylsilylhydroxylamine (30 mmol) were sprayed at room temperature into a suspension of 1.38 g of ethyl 4-hydroxy-7-nitro-2-oxo-1,2-dihydro-quinoline-3 -carboxylate (5 mmol) in 40 ml of dioxan. After heating to 100° C. all passed slowly into solution. The reaction mixture was left to stir at 90° C. for 20 hrs., cooled to room temperature and the separated voluminous precipitate was filtered off. This was washed with water and dried in a high vacuum. 740 mg of 4,N-dihydroxy-7-nitro-2-oxo-1,2-dihydro-quinoline-3-carboxamide (65%) were obtained as pale beige crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688803
Source datasetuspto-grants-1997_11
ORD IDord-d54afb4fa48e4259a4db5f9bca58e54b
Source noteuspto-grants-1997_11