HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096707Generated: November 1, 2026
Hydroxyamine hydrochloride → HCID 66781584, compound
https://huagongshe.com/reaction/1096707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59779113 | HCID 59779113 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66781584 | HCID 66781584 | — |
Reaction Steps
To a solution of 5-p-tolyl-bicyclo[3.1.0]hexan-2-one (100 mg, 0.54 mmol) and anhydrous NaOAc (87.5 mg, 1.1 mmol) in anhydrous MeOH (10 mL) was added with stirring NH2OH.HCl (69.5 mg, 1 mmol). The resulting mixture was stirred at room temperature for 18 h. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue, dioxime [IS THIS CORRECT?] was reconstituted in anhydrous MeOH (5 ml) and anhydrous NiCl2 (194 mg, 1.5 mmol) was added with stirring. The reaction mixture was cooled to −30° C. and NaBH4 (567 mg, 15 mmol) was added in small portions. After completion of the addition the mixture was allowed to warm to room temperature and concentrated in vacuo. This was then basified with aqueous solution of NaOH and extracted with CH2Cl2 (3×). Organic phases were concentrated and purified by silica gel chromatography. The oily product was converted to HCl salt (62 mg, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138377B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-8c5edd60ef5c465083659a9d2930d129 |
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| Source note | uspto-grants-2012_03 |
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