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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923567Generated: October 31, 2026

Potassium Carbonate → tert-Butyl (4-cyanobenzyl)glycinate

https://huagongshe.com/reaction/923567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
Reactant[2-[(2-Methylpropan-2-yl)oxy]-2-oxoethyl]azanium chlorideHCID 11095016—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-Butyl (4-cyanobenzyl)glycinateHCID 1800019869%

Reaction Steps

A solution of 2-(tert-butoxy)-2-oxoethanaminium chloride (3.00 g, 17.9 mmol) and potassium carbonate (4.95 g, 35.8 mmol) in DMF (20 mL) was stirred at room temperature for 2 min. To the reaction mixture was added 4-(bromomethyl)benzonitrile (3.19 g, 16.3 mmol) and stirring continued for 12 h. The reaction mixture was diluted with water (50 mL) and extracted with EA (3×20 mL). The combined organic extract was dried over MgSO4 then concentrated. Purification of the crude product by a silica gel column (DCM/MeOH) gave 2.77 g (68%) of tert-butyl 2-((4-cyanobenzyl)amino)acetate INT-31 as a yellow oil. LCMS-ESI (m/z) calculated for C14H18N2O2: 246; found 247 [M+H]+, tR=0.92 min (Method 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278910B2
Source datasetuspto-grants-2016_03
ORD IDord-ea4ae8c4ccc0429898beb5e26d7d1b45
Source noteuspto-grants-2016_03