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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044759Generated: November 1, 2026

Ammonia → (E)-2-methyl-3-phenylacrylamide

https://huagongshe.com/reaction/1044759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantNitrogenHCID 947—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant2-Methyl-3-phenylprop-2-enoic acidHCID 14541—
SolventTetrahydrofuranHCID 8028—
Product(E)-2-methyl-3-phenylacrylamideHCID 6243942—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of alpha-methylcinnamic acid (19.0 g, 116 mmol) and Et3N (17.1 mL, 122 mmol) in dry THF (500 mL) was treated with ethyl chloroformate (11.4 mL, 117 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 15 min then aq. NH3 (250 mL) in THF (150 mL) was added. The reaction mixture was vigorously stirred at 0° C. for 30 min and at rt for 1 h30. The layers were then separated, the aq. layer extracted with CH2Cl2 (2×) and the combined organic extracts were concentrated under reduced pressure. The residue was partitioned between water and CH2Cl2, the layers separated and the aq. layer extracted with CH2Cl2 (2×). The combined org. extracts were dried (MgSO4), filtered and concentrated under reduced pressure to give the title compound as a white solid. LC-MS-conditions 01: tR=0.75 min; [M+H]+=162.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-e42e0ad3d7f64f79896921483ed7a0e3
Source noteuspto-grants-2013_10