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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053587Generated: October 30, 2026

Hexane → HCID 86596336, compound

https://huagongshe.com/reaction/2053587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant2-Methyl-cis-4,5-diphenyl-4,5-dihydro-imidazole-1-carboxylic Acid, Tert-Butyl EsterHCID 86596335—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86596336HCID 8659633645.8%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a cold (−70° C.) solution of 2-methyl-cis-4,5-diphenyl-4,5-dihydro-imidazole-1-carboxylic acid, tert-butyl ester (253) (3.36 g, 10.0 mmol) in THF is added 1.6M n-butyl lithium in hexane (6.9 mL, 11.0 mmol), and the mixture is stirred for 1 h at −70° C. To the reaction mixture is added 4-fluorobenzaldehyde (1.18 mL, 11.0 mmol), and the mixture is stirred for 1 h at −70° C. and 1 h at RT. To the reaction mixture is added ammonium chloride solution, EtOAc, and the organic layer is separated, and washed with brine, dried (MgSO4), and filtered. The filtrate is rotary evaporated, and the residue purified by chromatography on silica gel; elution with dichloromethane: EtOAc (9:1) gives 2.11 g of the product 256. 1H NMR (CDCl3) δ 7.60-7.45 (m, 2H), 7.15-6.90 (m, 10H), 6.85-6.60 (m, 2H), 5.70-5.20 (m, 4H), 3.60-3.10 (m, 2H), 1.18 (s, 9H); MS: m/z 461 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326792B2
Source datasetuspto-grants-2008_02
ORD IDord-83536ffcb98547aa82abfde498e61233
Source noteuspto-grants-2008_02