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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918087Generated: October 25, 2026

Diphenylmethylidenehydrazine → 3-(2-(Diphenylmethylene)hydrazinyl)-2-methylpyridine

https://huagongshe.com/reaction/1918087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylmethylidenehydrazineHCID 79304—
Reactant3-Bromo-2-methylpyridineHCID 1201003—
ReactantSodium t-butoxideHCID 23676156—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
SolventTolueneHCID 1140—
Product3-(2-(Diphenylmethylene)hydrazinyl)-2-methylpyridineHCID 8665353375%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-Bromo-2-methyl-pyridine (1.0 g, 5.80 mmol) in 15 mL dry toluene was treated with benzophenone hydrazone (1.25 g, 6.39 mmol), 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene (170 mg, 0.29 mmol), sodium tert-butoxide (835 mg, 8.70 mmol), and Pd(II)(OAc)2 (67 mg, 0.30 mmol). Heated to 120° C. in the microwave for five minutes. Extracted using EtOAc/H2O (3×100 mL EtOAc, 1×100 mL H2O, 1×100 mL brine). Dried using Na2SO4 and then purified by flash chromatography (silica, 10-50% EtOAc/Hexane) to afford 3-(2-(diphenylmethylene)hydrazinyl)-2-methylpyridine (1.25 g, 4.35 mmol, 75%). 1H NMR (300 MHz, DMSO-d6) δ 7.95 (d, 1H), 7.85 (d, 1H), 7.70-7.53 (m, 6H), 7.45-7.34 (m, 5H), 7.20 (d, 1H), 2.07 (s, 3H); LC-MS (ESI) m/z 288 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-0f3b4f7e539d4712ac34b7f77a859fda
Source noteuspto-grants-2013_12