HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366021Generated: October 28, 2026
Sodium hydride → 1-(2,2-Diethoxyethyl)-1H-indole-2,3-dione 3-(O-methyloxime)
https://huagongshe.com/reaction/366021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | HCID 136067498 | HCID 136067498 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2,2-Diethoxyethyl)-1H-indole-2,3-dione 3-(O-methyloxime) | HCID 53942106 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127544 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-d53abc1ac15c4e8886cb4e0643fc00b0 |
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| Source note | uspto-grants-2000_10 |
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