HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414203Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 13670591, compound
https://huagongshe.com/reaction/414203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | HCID 54410625 | HCID 54410625 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 13670591 | HCID 13670591 | — |
Reaction Steps
15.9 g hydrazine hydrochloride and 18.4 ml hydrazine hydrate are added under stirring to 22.5 g of the product of step (a) in 20 ml n-propanol and the obtained reaction mixture is heated under reflux for 5 hours. The mixture is concentrated, treated with 500 ml H2O, filtered and washed with H2O (fraction A). The mother liquor is extracted with ethyl acetate and the extract evaporated. To the residue (7.5 g) are added 100 ml n-propanol and 20 ml triethylamine and the mixture is stirred and heated at reflux. The reaction is followed by thin layer chromatography. After approximately 15 hours when all of the β-product is converted into the 8α-product, H2O is added and the mixture is filtered. The filter cake is combined with fraction A and recrystallized twice from hot ethanol to afford the heading compound, m.p. 235°-240°, which is the pure α-isomer by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04791115 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-a66c2d9c52ba4bfda73c5c6196343d47 |
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| Source note | uspto-grants-1988_12 |
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