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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749039Generated: October 28, 2026

Potassium tert-butoxide → HCID 22347175, compound

https://huagongshe.com/reaction/749039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178514377HCID 178514377—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 22347175HCID 2234717525.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N1-(4-bromophenyl)-2-fluoro-1-benzenecarbohydrazonamide (1.2 g, 0.00391 mol) in N-methyl pyrrolidinone (25 mL), potassium tert-butoxide (0.50 g, 0.0041 mol) was added and the resulting solution was heated at 100° C. under an atmosphere of nitrogen for 3 hours. The reaction mixture was cooled to ambient temperature, the solvent was removed under reduced pressure and the residue partitioned between saturated solution of sodium bicarbonate in water (50 mL) and ethyl acetate (50 mL). The organic phase was washed with brine, dried with magnesium sulfate and concentrated. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (1:5) as mobile phase to yield N-(4-bromophenyl)-N-(1H-3-indazolyl)amine (0.29 g, 0.0010 mol) as a white solid. 1H NMR (DMSO-d6, 400 MHz), δ 12.06 (s, 1H), 9.03 (s, 1H), 7.93 (d, 1H), 7.65 (d, 2H), 7.35 (m, 4H), 7.03 (dd, 1H). TLC (ethyl acetate/heptane 1:3) Rf 0.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07400979B2
Source datasetuspto-grants-2008_07
ORD IDord-5debf509905a43c38616fb202dd6ba2f
Source noteuspto-grants-2008_07