Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920859Generated: November 1, 2026

Dimethylformamide → HCID 57969743, compound

https://huagongshe.com/reaction/1920859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium ChlorideHCID 433294—
Reactant1-(3,5-Dibromophenyl)cyclopropane-1-carbonitrileHCID 67069996—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 57969743HCID 5796974383.2%

Reaction Conditions

Temperature-20 °C

Reaction Steps

LiCl in THF (5.429 mL of 14% w/v, 5.233 mmol) was placed in an oven-dried 3-necked flask under nitrogen. The flask was cooled to −20° C. and 1-(3,5-dibromophenyl)cyclopropane-1-carbonitrile (1.5 g, 4.984 mmol) was added in one portion. The temperature was maintained between −20 and −10° C. for 90 minutes. DMF (400.7 mg, 424.5 μL, 5.482 mmol) was then added and the reaction allowed to warm to room temperature overnight. NH4Cl (sat. aq. soln.) was added followed by ethyl acetate and water. The mixture was extracted three times with ethyl acetate, the combined organics dried over MgSO4 and the solvent removed under reduced pressure. The crude product was purified on silica (Companion, 24 g) eluting with 2-30% EtOAc:Petrol ether to give 1-(3-bromo-5-formyl-phenyl)cyclopropane-1-carbonitrile as a white solid (1.037 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173635B2
Source datasetuspto-grants-2012_05
ORD IDord-fc661d98faeb492d9b8df5101c8c2f0c
Source noteuspto-grants-2012_05