HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656599Generated: October 29, 2026
N-Hydroxyphthalimide → O-[2-(Morpholin-4-yl)ethyl]hydroxylamine
https://huagongshe.com/reaction/656599
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | O-[2-(Morpholin-4-yl)ethyl]hydroxylamine | HCID 13127327 | 63.2% |
Reaction Steps
To a solution of 2-morpholinoethanol (5 g, 38 mmol) in CH2Cl2 (250 mL) was added 2-hydroxyisoindolin-1,3-dione (9.3 g, 57 mmol) and triphenylphosphine (15 g, 57 mmol). The resultant mixture was cooled to 0° C. and diisopropyl azodicarboxylate (11 ml, 57 mmol) was slowly added drop wise with an addition funnel under N2 atmosphere. The reaction mixture was stirred at ambient temperature for 48 h. The reaction mixture was concentrated to provide clear oil, which was purified by flash chromatography (50% EtOAc-Hexane). The resultant clear oily compound was dissolved in CH2Cl2 (50 ml). Hydrazine hydrate (5.8 mL, 76 mmol) was added. The reaction mixture was stirred at ambient temperature for 8 h. The resultant solid was filtered off and the filtrate concentrated under reduced pressure to provide a clear oil of O-(2-morpholinoethyl)hydroxylamine (3.5 g, 24 mmol). [M+H] calc'd for C6H14N2O2, 147. found, 147.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071766B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-e8208ddaf38440789f8cdb67c6fb5321 |
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| Source note | uspto-grants-2011_12 |
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