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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193225Generated: November 1, 2026

Dimethylformamide → HCID 86663664, compound

https://huagongshe.com/reaction/1193225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 59445916HCID 59445916—
ReactantHCID 178418365HCID 178418365—
SolventEther tetrahydrofuranHCID 21868444—
ProductHCID 86663664HCID 8666366476.1%

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a solution of 4-bromo-4′-chloro-3-iodobiphenyl (4.80 g, 0.012 mol) (described in WO 2008/071405) in anhydrous diethyl ether/tetrahydrofuran (120 ml, 1:1 ratio) at −75° C. is added isopropyl magnesium bromide (18.96 ml, 15% solution in tetrahydrofuran) dropwise such as to maintain an internal temperature below −70° C. Once addition is complete the reaction mixture is stirred at −75° C. for 2 hours, then warmed to −45° C. Anhydrous N,N-dimethylformamide (1.71 g, 0.0184 mol) is next added dropwise, maintaining temperature below −40° C., followed by warming to room temperature and quenching with 2M hydrochloric acid (60 ml). The reaction mixture is further diluted with diethyl ether, the two phases separated, and the aqueous phase extracted with additional diethyl ether. The combined organic extracts are washed with brine, dried over magnesium sulfate, filtered and the filtrate concentrated in vacuo. The crude product is purified by flash column chromatography (2% ethyl acetate in hexane eluant) to afford 4-bromo-4′-chloro-biphenyl-3-carbaldehyde (2.7 g, 75%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680299B2
Source datasetuspto-grants-2014_03
ORD IDord-ab499131e93d48ce92a9e6768323866a
Source noteuspto-grants-2014_03