HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113248Generated: October 30, 2026
Hydrochloric Acid → 1-Hydroxylamino-2-phenylethane
https://huagongshe.com/reaction/2113248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | beta-nitrostyrene, (E)- | HCID 5284459 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Hydroxylamino-2-phenylethane | HCID 165091 | — |
Reaction Steps
To a THF solution (1.1 mL, 1.0 M) of BH3-THF (1.1 mmol) was added dropwise a THF solution (2.2 mL) of trans-β-nitrostyrene (160.0 mg, 1.1 mmol) at 0° C. under nitrogen atmosphere. NaBH4 (3.3 mg, 0.087 mmol) was added, and the mixture was stirred for 20 minutes at room temperature. Water (5 mL) was added at 0° C., and then the solution was made acidic by adding 2M HCl aqueous solution, and the solution was stirred for 4 hr at 65° C. The reaction mixture was extracted with ethyl acetate, and the aqueous layer was further extracted with ethyl acetate after the addition of 15% NaOH aqueous solution and NaCl. The organic layers were dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was purified by flush column chromatography (chloroform:methanol=1:0→10:1) to obtain the objective substance (62.7 mg, 43%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524980B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-5c7bbfe7a34d44e690fa30cc99c3d361 |
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| Source note | uspto-grants-2009_04 |
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