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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454447Generated: October 30, 2026

Acetic Acid → ethyl 2-amino-4-(tetrahydro-4H-pyran-4-ylidene)butanoate

https://huagongshe.com/reaction/454447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactantethyl 2-[(diphenylmethylidene)amino]-4-(tetrahydro-4H-pyran-4-ylidene)butanoateHCID 58313138—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-amino-4-(tetrahydro-4H-pyran-4-ylidene)butanoateHCID 5831306079.4%

Reaction Steps

To a solution of ethyl 2-[(diphenylmethylidene)amino]-4-(tetrahydro-4H-pyran-4-ylidene)butanoate (162) (6.8 g, 18.0 mmol) in THF (30 mL) was added water (30 mL) and glacial acetic acid (20 mL) and the reaction stirred at room temperature for 2.5 h. The reaction was concentrated in vacuo and the residue dissolved in 0.1 N HCl. It was extracted twice with ethyl acetate and the organic layer was discarded. To the aqueous layer was added solid potassium carbonate until the solution gave blue pH paper. The aqueous layer was extracted with 15% isopropanol/dichloromethane (3×) and the organic layer dried over sodium sulfate and concentrated in vacuo to afford the title compound as a clear oil (3.05 g, 79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492554B2
Source datasetuspto-grants-2013_07
ORD IDord-760e9a119e184c169cd0849c4ba276ae
Source noteuspto-grants-2013_07