HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231412Generated: November 1, 2026
HCID 14501787, compound → HCID 13934988, compound
https://huagongshe.com/reaction/231412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14501787 | HCID 14501787 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13934988 | HCID 13934988 | 10.4% |
Reaction Steps
A solution of 2-[(5-amino-2,4-dichlorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone (16.3 g, 0.564 mole) in concentrated hydrochloric acid (75 ml) was cooled to 0° C., and a solution of sodium nitrite (3.9 g, 0.564 mole) in water (50 ml) was added dropwise with the tip of the addition funnel below the surface of the solution. The reaction mixture temperature was kept below 2° C. during the addition. Upon completion of addition, the reaction mixture was stirred at 0° C. for 30 minutes, and then stannous chloride (28 g, 0.124 mole) in concentrated hydrochloric acid (50 ml) was added dropwise maintaining the temperature below 2° C. The reaction mixture was stirred for one hour at 0° C., and then a tan solid was removed by filtration to yield 10.0 g of [2,4-dichloro-5-[(4,4-dimethyl-3-oxoisoxazolidin-2-yl)methyl]phenyl]hydrazine hydrochloride; m.p. 202°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04846875 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-8f0a7fbaf2504bdb8a21db08c851099d |
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| Source note | uspto-grants-1989_07 |
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