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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (3,5-Difluoro-4-nitrophenyl)methanol | HCID 55271003 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-(Bromomethyl)-1,3-difluoro-2-nitrobenzene | HCID 57386306 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08093406B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-38dbef6ab78942f8aa885838e8db11bb |
|---|
| Source note | uspto-grants-2012_01 |
|---|