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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535145Generated: October 29, 2026

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

https://huagongshe.com/reaction/535145

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 numberUS08853416B2
Source datasetuspto-grants-2014_10
ORD IDord-9e396090a48b4426b00260435c99b6b5
Source noteuspto-grants-2014_10