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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952450Generated: November 3, 2026

2-Chloroethanol → 4-Bromo-1-(2-chloroethyl)-1H-pyrazole

https://huagongshe.com/reaction/1952450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantTriphenylphosphineHCID 11776—
Reactant4-BromopyrazoleHCID 16375—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-1-(2-chloroethyl)-1H-pyrazoleHCID 51892074—

Reaction Steps

To a solution of 4-bromo-1H-pyrazole (5 g, 34.02 mmol), 2-chloroethanol (2.7 mL, 40.82 mmol) and PPh3 (10.71 g, 40.82 mmol) and in THF (68 mL) at 0° C. was added DEAD (6.4 mL, 40.8 mmol). The mixture was allowed to warm-up to room temperature and stirred overnight. It was then concentrated under reduced pressure, the residue was treated with ether and the resultant suspension was filtered. The filtrate was collected and concentrated under reduced pressure to afford the title compound 75 which was used in the next step without further purification. MS (m/z). 209.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404846B2
Source datasetuspto-grants-2013_03
ORD IDord-c9b55860f6cb4911b4114ad32a1ef24f
Source noteuspto-grants-2013_03