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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157384Generated: October 26, 2026

Cesium carbonate → Tert-butyl N-[(4-cyanophenyl)methyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate

https://huagongshe.com/reaction/1157384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
ReactantDi-tert-butyl IminodicarboxylateHCID 279800—
CatalystLithium iodideHCID 66321—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl N-[(4-cyanophenyl)methyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamateHCID 368376883.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-(Bromomethyl)benzonitrile (5 g, 25.5 mmoles) and di-tert-butyliminodicarboxylate (5.54 g, 25.5 mmoles) were dissolved in anhydrous THF (50 mL) and cesium carbonate (16.62 g, 25.5 mmoles) and lithium iodide (170.5 mg, 1.275 mmoles) were added. The mixture was stirred at 70° C. for 23 h and the reaction was worked up as described in Preparative Example 244, Step B above. The residue was chromatographed on a silica gel column (50×5 cm) using 5% ethyl acetate in hexane as the eluant to give 4-(di-tert-butoxycarbonylaminomethyl)benzonitrile (7.07 g, 83%): FABMS: m/z 333.2 (MH+); HRFABMS: m/z 333.1816 (MH+). Calcd. for C18H25N2O4: m/z 333.1814; δH (CDCl3) 1.45 (18H, s, —COOC(CH3)3), 4.81 (2H, s, CH2), 7.37 (2H, d, Ar—H) and 7.62 ppm (2H, d, Ar—H); δC (CDCl3) CH3, 28.1, 28.1, 28.1, 28.1, 28.1, 28.1; CH2, 49.2; CH, 127.8, 127.8, 132.3, 132.3; C, 83.2, 83.2, 111.1, 118.9, 144.1, 152.4, 152.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807683B2
Source datasetuspto-grants-2010_10
ORD IDord-342e233134ed4d429609eaf3d2ee1b9f
Source noteuspto-grants-2010_10