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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133812Generated: October 25, 2026

Acetic Acid → Ethyl (2Z)-3,4-dihydro-1(2H)-naphthalenylidene(formylamino)ethanoate

https://huagongshe.com/reaction/133812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-TetraloneHCID 68266—
ReactantEthyl isocyanoacetateHCID 533707—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (2Z)-3,4-dihydro-1(2H)-naphthalenylidene(formylamino)ethanoateHCID 5973609245%

Reaction Steps

To a stirred slurry of potassium t-butoxide (4.7 g, 42.0 mmol) in 30 mL tetrahydrofuran at 0° C. is added ethyl isocyanoacetate (4.53 g, 40.0 mmol). This is stirred for 30 mins whereupon a solution of β-tetralone (5.88 g, 40.0 mmol) in tetrahydrofuran (20 mL) is added dropwise. The reaction mixture is allowed to warm to room temperature and stirred for 3 hours. The reaction mixture is then recooled in an ice bath and to this is added acetic acid (2.5 g, 41.6 mmol), allowed to warm to room temperature and stirred for an additional 30 mins. The solvent is removed in-vacuo and the residue partitioned between water and ethyl acetate. The organic layer is washed with water and brine, dried over sodium sulfate, filtered, evaporated and crystallized from cyclohexane to give 4.67 g of a white solid (contains some E-isomer), MS: m/z 260.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390910B2
Source datasetuspto-grants-2008_06
ORD IDord-a8160e7125b049a2b8a174406f9a3c0f
Source noteuspto-grants-2008_06