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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420301Generated: October 31, 2026

Methanol → 5-(Bromomethyl)-1,3-difluoro-2-nitrobenzene

https://huagongshe.com/reaction/420301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPhosphorus tribromideHCID 24614—
ReactantSodium BicarbonateHCID 516892—
Reactant(3,5-Difluoro-4-nitrophenyl)methanolHCID 55271003—
SolventDiethyl EtherHCID 3283—
Product5-(Bromomethyl)-1,3-difluoro-2-nitrobenzeneHCID 57386306—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of PBr3 (7.04 mL, 73 mmol) in Et2O (200 mL) is added under argon at 0° C. a solution of (3,5-difluoro-4-nitro-phenyl)-methanol (9.3 g, 48.7 mmol) in Et2O (200 mL). The reaction mixture was allowed to warm to 25° C. and stirred for 24 h at 25° C. After the addition of MeOH (5 mL) at 0° C., the reaction mixture was poured onto cold aq. NaHCO3 solution and the product was extracted with EtOAc. Combined organic extracts were washed with saturated NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated to provide the title compound after filtration through a plug of silicagel with hexane-EtOAc 3:1 as a yellow solid: TLC (hexane-EtOAc 3:1) Rf=0.40; HPLC RtA=2.01 min; 1H NMR (400 MHz, CDCl3): δ 7.14 (d, 2H), 4.40 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-38dbef6ab78942f8aa885838e8db11bb
Source noteuspto-grants-2012_01