HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376407Generated: October 26, 2026
Hydroxyamine hydrochloride → (S)-4-dibenzofuran-2-yl-4-hydroxyimino-2-(2,2,2-trifluoroacetylamino)-butyric acid
https://huagongshe.com/reaction/376407
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | (S)-4-dibenzofuran-2-yl-4-oxo-2-(2,2,2-trifluoroacetylamino)-butyric acid | HCID 54131944 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-4-dibenzofuran-2-yl-4-hydroxyimino-2-(2,2,2-trifluoroacetylamino)-butyric acid | HCID 86755099 | 12.7% |
Reaction Steps
To a solution of (S)-4-dibenzofuran-2-yl-4-oxo-2,2,2-trifluoroacetylamino)-butyric acid (1.0 g, 0.0026 mol) from Example 1 in 50 mL of methanol was added sodium acetate trihydrate (1.08 g, 0.0079 mol). The solution was stirred at 24° C. while an aqueous solution (5 mL) of hydroxylamine hydrochloride (0.37 g, 0.00527 mol) was added in one portion. The reaction mixture was stirred for 3 hours at 24° C., and then heated to reflux for 2 hours. The solution was cooled to 24° C. and concentrated to dryness by evaporation under reduced pressure. The solid was rinsed with 10 mL of water, and crystallized from ethyl acetate and hexane to afford 0.13 g of (S)-4-dibenzofuran-2-yl-4-hydroxyimino-2-(2,2,2-trifluoroacetylamino)-butyric acid; mp 128-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06020366 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-3a58cdb5eb524fb881f3b36b228bd0ca |
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| Source note | uspto-grants-2000_02 |
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