Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[4-(Benzyloxy)-2-hydroxy-3-nitrophenyl]ethan-1-oneHCID 57988991—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product1-(3-Amino-4-(benzyloxy)-2-hydroxyphenyl)ethanoneHCID 5798925297.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017602B2
Source datasetuspto-grants-2011_09
ORD IDord-a922e1c2bb5d47f1adccbf721ff18f8e
Source noteuspto-grants-2011_09