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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994098Generated: October 30, 2026

Iodine → HCID 59133922, compound

https://huagongshe.com/reaction/1994098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 59133866HCID 59133866—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59133922HCID 59133922100%

Reaction Conditions

Temperature-45 °C

Reaction Steps

To a solution of methyl 1-(1-methylethyl)-3-methyl-1H-pyrazole-4-carboxylate (2.00 g, 11.0 mmol) in dry tetrahydrofuran (22.0 mL) at −78° C., 2 M solution of butyllithium (6.04 mL, 12.1 mmol) in pentane was added dropwise. The reaction mixture was then warmed to −45° C. and stirred for 1 h. It was then cooled to −78° C. and a solution of iodine (3.06 g, 12.1 mmol) in THF (11.0 mL) was added. The reaction mixture was warmed to RT and stirred for 1 h. Then it was quenched with saturated NH4Cl solution and extracted with ethyl acetate (2×25 mL). The organic layers were combined, washed with brine and dried (MgSO4). Evaporation of solvent gave a tan solid as title compound (3.38 g, 11.0 mmol, 100% crude yield). MS m/z 309 (MH+); 1H NMR (500 MHz, CHLOROFORM-D) δ ppm 1.41 (d, 6H) 2.47 (s, 3H) 3.82 (s, 3H) 4.77 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652004B2
Source datasetuspto-grants-2010_01
ORD IDord-5684a659ebc54af2b5643b571b8b811c
Source noteuspto-grants-2010_01