HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465252Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 21244208, compound
https://huagongshe.com/reaction/465252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 14230770 | HCID 14230770 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21244208 | HCID 21244208 | 90.2% |
Reaction Steps
In 80 ml of methylene chloride is dissolved 7.68 g of N-[1-methyl-1-(p-nitrobenzyloxycarbonyl)ethyloxy]phthalimide and under ice-cooling and stirring 0.97 ml of hydrazine hydrate is added. The mixture is stirred at room temperature for 2 hours, after which 0.97 ml of hydrazine hydrate is further added. The mixture is stirred for 3 hours and the resultant crystalline precipitate is separated by filtration and washed with methylene chloride. The filtrate and washings are combined and further washed with diluted aqueous ammonia and water in this order, and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is chromatographed on a silica gel column [silica gel: 300 g; eluent: ethyl acetate-hexane (1:1)] to give 4.58 g of O-[1-methyl-1-(p-nitrobenzyloxycarbonyl)ethyl]hydroxylamine as a yellow oil. This product solidifies on cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04550105 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-c2c4b8a9fa4f4b7c80a86ae5b273787c |
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| Source note | uspto-grants-1985_10 |
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