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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (3-iodo-1-isopropyl-1H-pyrazol-4-yl)methanol | HCID 67491601 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(bromomethyl)-3-iodo-1-isopropyl-1H-pyrazole | HCID 67491708 | 51.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181252B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-34c640cbdecc4487a31b716e1f76cf4a |
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| Source note | uspto-grants-2015_11 |
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