HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710168Generated: November 1, 2026
N-Hydroxyphthalimide → HCID 14880862, compound
https://huagongshe.com/reaction/1710168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(3-Chloropropyl)dibutylamine | HCID 96084 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14880862 | HCID 14880862 | 96.6% |
Reaction Steps
To a suspension of 1.75 g of sodium hydride in ml of N,N-dimethylformamide was added a mixture of 11.9 g of N-hydroxyphthalimide and 60 ml of N,N-dimethylformamide, and then the mixture was stirred for minutes. To the reaction solution was added a mixture of 15 g of 3-chloropropyldibutylamine and 10 ml of N,N-dimethylformamide, and then the mixture was heated at reflux for 5 hours. After evaporation of the solvent, ethyl acetate was added to the residue, and the mixture was washed with water. Evaporation of the solvent gave 23.4 g of N-(3-dibutylaminopropoxy)-phthalimide, which was then dissolved in 200 ml of methylene chloride. To the solution was added 20 ml of hydrazine monohydrate, and the mixture was stirred at room temperature for 3 hours. After removal of the insolubles by filtration, the filtrate was concentrated under reduced pressure and distilled under reduced pressure to give 10.3 g of O-(3-dibutylaminopropyl)hydroxylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04952689 |
|---|
| Source dataset | uspto-grants-1990_08 |
|---|
| ORD ID | ord-bc6d9cd67fb04e099398d912d6e3640c |
|---|
| Source note | uspto-grants-1990_08 |
|---|