Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179479Generated: November 1, 2026

Dimethylformamide → Isopropyl 3,5-difluoro-4-formylphenylcarbamate

https://huagongshe.com/reaction/1179479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantIsopropyl 3,5-difluoro-phenylcarbamateHCID 58978077—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductIsopropyl 3,5-difluoro-4-formylphenylcarbamateHCID 58978110—

Reaction Conditions

Temperature-20 °C

Reaction Steps

n-Butyllithium (2.5M in hexane, 112 mL, 0.279 mol) was added dropwise at −78° C. to a solution of isopropyl 3,5-difluoro-phenylcarbamate (20 g, 0.093 mol) and N,N,N,N-tetramethylethylenediamine (32 mL, 0.214 mol) in 93 mL of THF, and stirred for 30 min. Dimethylformamide (10.8 mL, 0.140 mol) was then added dropwise at −78° C., stirred for 1 h, and allowed to warm to −20° C. The reaction was then quenched with saturated aqueous ammonium chloride (100 mL). The reaction mixture was extracted with ethyl acetate, the extracts washed with brine, dried (MgSO4), and concentrated. The crude product was triturated with hexane to provide the title compound. The combined hexane washings were concentrated and purified by flash column chromatography (30% ethyl acetate/hexane) to provide additional product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279494B2
Source datasetuspto-grants-2007_10
ORD IDord-3045476fa7ab4bdb901c364235bc4af1
Source noteuspto-grants-2007_10