HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909866Generated: November 1, 2026
1-[4-(Benzyloxy)-2-hydroxy-3-nitrophenyl]ethan-1-one → 1-(3-Amino-4-(benzyloxy)-2-hydroxyphenyl)ethanone
https://huagongshe.com/reaction/909866
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-[4-(Benzyloxy)-2-hydroxy-3-nitrophenyl]ethan-1-one | HCID 57988991 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(3-Amino-4-(benzyloxy)-2-hydroxyphenyl)ethanone | HCID 57989252 | 97.4% |
Reaction Steps
Zinc dust (5.5 g) was added portionwise to a suspension of 1-(4-(benzyloxy)-2-hydroxy-3-nitrophenyl)ethanone (5.5 g) in acetic acid (55 mL) over 15 min, whilst maintaining the internal temperature below 40° C. with an ice bath. The mixture was allowed to attain ambient temperature and stirred for a further 2 h. The mixture was filtered through Celite (caution gets hot, do not allow to dry), washed with acetic acid, and the filtrate poured onto ice/water (500 mL). The resulting precipitate was filtered off, washed with water, and dried under vacuum at 40° C. to afford the subtitled compound as a light brown solid (4.8 g). 1H NMR (300 MHz, DMSO-d6) δ 7.53 (m, 2H), 7.48-7.33 (m, 3H), 7.28 (d, J=9.0 Hz, 1H), 6.72 (d, J=9.0 Hz, 1H), 5.29 (s, 2H), 2.59 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017602B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a922e1c2bb5d47f1adccbf721ff18f8e |
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| Source note | uspto-grants-2011_09 |
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