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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533742Generated: November 3, 2026

Sodium hydride → 1-(2,2-Diethoxyethyl)-1H-indole-2,3-dione 3-(O-methyloxime)

https://huagongshe.com/reaction/1533742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantHCID 136067498HCID 136067498—
SolventDimethylformamideHCID 6228—
Product1-(2,2-Diethoxyethyl)-1H-indole-2,3-dione 3-(O-methyloxime)HCID 5394210697%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of sodium hydride (prepared by washing 50 g of 60% oily sodium hydride with hexane) in 1 l of N,N-dimethylformamide was added dropwise a solution of 176 g of 3-methoxyiminoindolin-2-one in 3 l of N,N-dimethylformamide at 0° C. in a nitrogen stream. To the mixture were added 1 l of N,N-dimethylformamide and 330 ml of bromoacetaldehyde diethyl acetal, and the mixture was heated to 70° C., at which it was stirred for 45 hours. The reaction mixture was concentrated, and the concentrate was diluted with ethyl acetate and washed with an aqueous solution of sodium chloride. The organic layer was dried over anhydrous sodium sulfate and concentrated to give 284 g (97%) of 1-(2,2-diethoxyethyl)-3-methoxyiminoindolin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207836B1
Source datasetuspto-grants-2001_03
ORD IDord-ef12bfb0f95544ba971bf855eb3702b2
Source noteuspto-grants-2001_03