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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453112Generated: October 30, 2026

Sodium Hydroxide → 1-Bromo-5-ethyl-4-methoxy-2-(phenylmethoxy)benzene

https://huagongshe.com/reaction/1453112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 58762417HCID 58762417—
SolventTriethylene GlycolHCID 8172—
Product1-Bromo-5-ethyl-4-methoxy-2-(phenylmethoxy)benzeneHCID 5876230141.5%

Reaction Conditions

Temperature170 °C

Reaction Steps

Sodium hydroxide (0.39 g, 9.7 mmol) and hydrazine monohydrate (0.57 mL, 11.7 mmol) were added to a solution of 1-(4-benzyloxy-5-bromo-2-methoxy-phenyl)-ethanone (1.3 g, 3.9 mmol) dissolved in triethylene glycol (5 mL). The reaction mixture was heated to 170° C. for 24 hours and then partitioned between 1N HCl and EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated. The residue was purified by flash silica gel chromatography (0% to 5% EtOAc in hexanes) to give the title compound (0.52 g, 40%). 1H NMR (400 MHz, CDCl3): δ 1.14 (t, J=7.3 Hz, 3H), 2.53 (q, J=7.3 Hz, 2H), 3.75 (s, 3H), 5.14 (s, 2H), 6.48 (s, 1H), 7.26 (s, 1H), 7.32 (m, 1H), 7.39 (m, 2H), 7.49 (d, J=8.3 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-778f86b3c280484785fa51ba8a9dc4cf
Source noteuspto-grants-2009_01