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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919901Generated: October 30, 2026

Methyl cyanoacetate → Tert-butyl 4-(1-cyano-2-methoxy-2-oxoethyl)benzoate

https://huagongshe.com/reaction/1919901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl cyanoacetateHCID 7747—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantTert-butyl 4-bromobenzoateHCID 11334366—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(1-cyano-2-methoxy-2-oxoethyl)benzoateHCID 57611881—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of Na3PO4 (9.84 g, 60.0 mmol), methyl cyanoacetate (2.38 g, 24.0 mmol), and tert-butyl 4-bromobenzoate (5.14 g, 20.0 mmol) were added Pd(dba)2 (575 mg, 1.00 mmol), toluene (60 mL), and P(t-Bu)3 (10% wt in hexanes, 11.56 mL, 3.89 mmol). After degassing for 20 minutes, the reaction was stirred at 80° C. for 16 h. The resulting mixture was diluted with EtOAc, washed with H2O and brine, dried (MgSO4), and concentrated. Flash chromatography on silica gel (0-15% EtOAc/hexanes) gave tert-butyl 4-(1-cyano-2-methoxy-2-oxoethyl)benzoate as a white solid. 1H NMR (CDCl3) δ8.02 (d, J=7.9 Hz, 2H), 7.51 (d, J=8.2 Hz, 2H), 4.79 (s, 1H), 3.79 (s, 3H), 1.58 (s, 9H). MS (ESI) calcd [M+H]+ 276.1, found 276.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168658B2
Source datasetuspto-grants-2012_05
ORD IDord-be64590c208e4a7fb8e97a49fc99172e
Source noteuspto-grants-2012_05