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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711028Generated: October 30, 2026

Phosphorus tribromide → 4-(bromomethyl)-3-iodo-1-isopropyl-1H-pyrazole

https://huagongshe.com/reaction/711028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
Reactant(3-iodo-1-isopropyl-1H-pyrazol-4-yl)methanolHCID 67491601—
SolventDichloromethaneHCID 6344—
Product4-(bromomethyl)-3-iodo-1-isopropyl-1H-pyrazoleHCID 6749170851.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (3-iodo-1-isopropyl-1H-pyrazol-4-yl)methanol (0.63 g, 2.37 mmol) in 20 mL dichloromethane was cooled to 0° C. Phosphorus(III)bromide (0.67 mL, 7.10 mmol) was added to the solution and the mixture was stirred 30 minutes at 0° C., 1 hour at room temperature, and then quenched with 50 mL water and stirred 15 minutes at room temperature. The mixture was treated with saturated aqueous sodium bicarbonate and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (50 mL), dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (10-80% ethyl acetate/heptanes, 25 g silica gel) to yield 400 mg of 4-(bromomethyl)-3-iodo-1-isopropyl-1H-pyrazole as a colorless solid. +APCI (M+H) 329.0; 1H NMR (400 MHz, CDCl3, δ): 7.42 (s, 1H), 4.47 (spt, J=6.7 Hz, 1H), 4.35 (s, 2H), 1.50 (d, J=6.6 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181252B2
Source datasetuspto-grants-2015_11
ORD IDord-34c640cbdecc4487a31b716e1f76cf4a
Source noteuspto-grants-2015_11