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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromobutane | HCID 6554 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-methoxy-1H-pyrazole | HCID 5324776 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Sec.-butyl-4-methoxypyrazole | HCID 13018405 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382947 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-dea0d5e4ed284266bcee492e9f1ef468 |
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| Source note | uspto-grants-1983_05 |
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