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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851148Generated: October 30, 2026

2-Bromobutane → 1-Sec.-butyl-4-methoxypyrazole

https://huagongshe.com/reaction/851148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobutaneHCID 6554—
ReactantTetrahydrofuranHCID 8028—
Reactant4-methoxy-1H-pyrazoleHCID 5324776—
SolventWaterHCID 962—
Product1-Sec.-butyl-4-methoxypyrazoleHCID 1301840542%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 23.6 g (0.21 mol) of potassium tert.-butylate, 19.6 g (0.2 mol) of 4-methoxypyrazole (for the preparation, see Archiv der Pharmazie 300 (1967), pages 704-708), 100 ml of tetrahydrofuran and 28.7 g (0.21 mol) of sec.-butyl bromide was stirred at 70° C. for 18 hours. 300 ml of water were then added and the mixture was extracted 3 times with 100 ml of chloroform each time. The combined organic phases were dried over sodium sulphate and evaporated in vacuo. 13.2 g (42% of theory) of 1-sec.-butyl-4-methoxypyrazole were obtained from the residue, by vacuum distillation, in the form of a colorless oil with a boiling point of 60° C./0.2 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382947
Source datasetuspto-grants-1983_05
ORD IDord-dea0d5e4ed284266bcee492e9f1ef468
Source noteuspto-grants-1983_05