Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357555Generated: November 1, 2026

Dimethylformamide → HCID 86607610, compound

https://huagongshe.com/reaction/2357555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPentaneHCID 8003—
ReactantHCID 20586739HCID 20586739—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86607610HCID 86607610—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cooled solution of N,N-diisopropyl [4-(2-methylphenyl)benzamide (5.50 g, 19 mmol) in anhydrous THF (50 mL) at −70° C. was added dropwise a solution of tert-butyllithium, 1.7 M in pentane (13 mL, 22 mmol). The yellow mixture was stirred at −78° C. for 30 min, after which dimethylformamide (5.7 mL, 74 mmol) was added dropwise such that the internal temperature was maintained at −70° C. The resultant mixture was stirred at this temperature over 15 min and then was allowed to warm to RT and stood for 40 min. The brown solution was quenched by slow addition of saturated aqueous NH4Cl (100 mL), keeping the internal temperature below 0° C. The resulting mixture was diluted with diethyl ether (100 mL), and stirred at RT for 10 min. The organic phase was separated and aqueous phase was extracted with diethyl ether (3×60 mL). The combined organic phases were washed with brine. The resulting organic solution was then dried over magnesium sulfate and concentrated under reduced pressure to give N,N-diisopropyl 2-formyl-4-(2-methylphenyl)benzamide as a yellow solid. MS (ESI, pos.ion) m/z: 324.2 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-597fec1eee1f4430a192c446a2764642
Source noteuspto-grants-2010_07