HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277481Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 23454144, compound
https://huagongshe.com/reaction/1277481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 23454124 | HCID 23454124 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23454144 | HCID 23454144 | — |
Reaction Steps
A solution of hydrazine hydrate (1.14 g; 22.8 mmol) and N-(1-methylhexyl)-2-phthalimidoacetamide (6.9 g; 22.8 mmol) in ethanol (50ml) was heated under reflux for 1 hour. It was then cooled to room temperature and evaporated in vacuo (Buchi, r.t.; then oil-pump, 0.5 mm/r.t./10 min.). The resultant semi-solid mixture was treated with dilutesulphuric acid (0.5 N; 85 ml) pre-cooled to 5°. The mixture was cooled to 0°, filtered and the precipitate mixed with more of the acid (2 N; 3×20 ml). The filtrate was kept in the refrigerator overnight and then filtered once more. After basification with sodium hydroxide solution (5 N; 40 ml), the mixture was extracted with dichloromethane (3×50 ml), the extracts dried (sodium sulphate) and evaporated in vacuo. The resultant oil was dried at 0.5 mm./r.t./0.5 h. T.l.c. (silica; chloroform:methanol: 3:2): 1 major spot, Rf. ca 0.5. I.v. and n.m.r. spectra were consistent with the structure. The product was purified as its hydrogen succinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04277498 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-d7336774e90e480badb5e16a17ede629 |
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| Source note | uspto-grants-1981_07 |
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