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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179484Generated: October 30, 2026

Dimethylformamide → 4-(Cbz-amino)benzaldehyde

https://huagongshe.com/reaction/1179484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl 4-bromophenylcarbamateHCID 561232—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(Cbz-amino)benzaldehydeHCID 12553763—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Benzyl 4-bromophenylcarbamate (20 g, 65.3 mmol) was taken in anhydrous THF (440 mL) and cooled to −78° C. To this solution, n-BuLi (55 mL, 137.2 mmol) was added dropwise and stirred for 0.5 h at −78° C. To this mixture, DMF (7.6 mL) was added dropwise and the reaction was allowed to warm to room temperature over a period of 5 h. The reaction mixture was quenched with 1 N HCl and then concentrated to remove THF, followed by addition of water. The mixture was extracted with three portions of ethyl acetate. The combined organic phases were washed with H2O, brine, and dried (MgSO4) filtered and concentrated. Trituration with hexanes and then with 20% ethyl acetate in hexanes afforded the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279494B2
Source datasetuspto-grants-2007_10
ORD IDord-95b06fa033a346b28d1ab4212403a9f4
Source noteuspto-grants-2007_10