HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594176Generated: October 26, 2026
N-Hydroxyphthalimide → HCID 69011018, compound
https://huagongshe.com/reaction/594176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromo-2-(chloromethyl)pyridine hydrochloride | HCID 53438200 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69011018 | HCID 69011018 | 96.5% |
Reaction Steps
To a mixture of 5-Bromo-2-chloromethyl-pyridine hydrochloride (63.7 g, 0.262 mol) and N-hydroxylphthalimide (64 g, 0.393 mol) in acetonitrile (400 mL) was placed in water bath and added N,N-diisopropylethylamine (182 mL, 1.05 mol) using dropping funnel for 10 min. It was heated at 65° C. for 4 hrs and evaporated off the solvent and extra base. Then, water (100 mL) was added to the reaction mixture and stirred for overnight. The resulting solid was filtered, washed with water (2×50 mL) and acetonitrile (100 mL). The white solid was dried on vacuum pump to provide the title compound (84.2 g, 84%) as a white solid. MS-ESI m/z 334.95 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242974B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-98b27e90719649be815003a0f810ae0b |
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| Source note | uspto-grants-2016_01 |
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