HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599466Generated: October 25, 2026
Hydrazine hydrate (1:1) → Benzyl 4-(hydroxyamino)benzoate
https://huagongshe.com/reaction/1599466
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Phenylmethyl 4-nitrobenzoate | HCID 84647 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 4-(hydroxyamino)benzoate | HCID 18928833 | — |
Reaction Steps
Hydrazine hydrate (containing 55% hydrazine, 1.5 mL, 26.25 mmol, 1.05 equiv.) was added dropwise over 1 minute to a mixture containing benzyl 4-nitrobenzoate (Brewster, J. H.; Ciotti, C. J., Jr. J. Am. Chem. Soc. 1955, 77, 6214; 6.43 g, 25 mmole, 1 equiv.), 5% rhodium on carbon (wet, 625 mg), and tetrahydrofuran (50 ml) at 0° C. under argon. When the addition was complete, the mixture was warmed to room temperature, stirred for 4 hours, and then was filtered through Celite®. Concentration of the filtrate gave crude benzyl 4-(hydroxyamino)benzoate as a yellow oil which was used without further purification. Pure benzyl 4-(hydroxyamino)benzoate, obtained from a separate preparation by silica gel chromatography (30% ethyl acetate/toluene) was used for characterization purposes: TLC(30% ethyl acetate/toluene) Rf 0.52; 1H NMR (250 MHz, CDCl3) δ 7.99 (d, J=8.6 Hz, 2 H), 7.26-7.55 (m, 5 H), 6.97 (d, J=8.6 Hz, 2H), 5.33 (s, 2H); IR (CHCl3) 3550, 3315, 1703, 1606, 1273, 1169, 1101, 693 cm-1 ; MS(DC/NH3) 261.2 (M+NH4)+, 245.2 (M+MH4 -16)+, 228.1 (M+H-16)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05741804 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-9e832134237844ac903c04e6a71a3348 |
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| Source note | uspto-grants-1998_04 |
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