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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375464Generated: October 30, 2026

1,4-Cyclohexadiene → HCID 59854970, compound

https://huagongshe.com/reaction/2375464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexadieneHCID 12343—
ReactantHCID 59854983HCID 59854983—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 59854970HCID 59854970—

Reaction Steps

To a solution of 405 mg (0.58 mmol) of 10-1 in 4 mL of EtOH was added 1.38 mL (14.6 mmol) of 1,4-cyclohexadiene, 100 mg of 10% palladium on carbon, and then stirred overnight. The reaction was filtered through Celite, concentrated, and the residue was dissolved in 3 mL of CH2Cl2. To this was added 3 mL of trifluoroacetic acid, stirring was maintained for 1 h, and then the mixture was partitioned between EtOAc and saturated aqueous NaHCO3 plus 25 mL of 5% aqueous Na2CO3, the organic phase was washed with NaHCO3 again, H2O, brine, dried over Na2SO4, and concentrated by rotary evaporation. The residue was loaded onto a silica gel column and eluted with EtOAc—20:1:1 EtOH/NH4OH/H2O to provide 10-2 as a white solid. There was an impurity of 5% subsequently removed by reverse phase chromatography with 95:5 to 5:95 H2O/CH3CN (both with 0.1% TFA). The fractions were basified with NaHCO3 to provide pure B-2 as a white solid. Data for 10-2: 1HNMR (500 MHz, CDCl3) δ 7.4-7.2 (m, 5H), 7.1-6.9 (mn, 3H), 6.3 (s, 1H), 5.2 (bs, 1H), 4.9 (m, 1H), 4.8-4.6 (m, 2H), 4.45 (m, 1H), 4.2-4.1 (m, 1H), 4.0 (m, 1H), 3.3-3.2 (mn, 2H), 3.1 (s, 3H), 2.85-2.7 (m, 2H), 2.1 (m, 1H), 1.7 (m, 2H) ppm. HRMS (ES) calc'd M+H for C24H26F3N3O2: 446.2050. Found: 446.2059.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465746B2
Source datasetuspto-grants-2008_12
ORD IDord-f1a15650b4cf41dba54df831b580a630
Source noteuspto-grants-2008_12