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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763590Generated: October 31, 2026

Tetrahydrofuran → HCID 12449510, compound

https://huagongshe.com/reaction/1763590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcrylateHCID 8821—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 12449500HCID 12449500—
SolventEthanolHCID 702—
ProductHCID 12449510HCID 12449510—

Reaction Steps

A solution of 52.3 g. of α-(α,α,α-trifluoro-p-tolyl)-4-morpholineacetonitrile in 500 ml. of dry tetrahydrofuran is stirred at ambient temperature while 1 ml. portions of 30% potassium hydroxide in ethanol and 25 ml. portions of ethyl acrylate is added every half hour until a total of 5 ml. of the base and 150 ml. of ethyl acrylate is added. After the addition, the mixture is stirred at ambient temperature for 48 hours. Following filtration, the filtrate is concentrated, dissolved in methylene chloride, passed through magnesol and recrystallized from methylene chloride/hexane to afford ethyl γ-cyano-γ(α,α,α-trifluoro-p-tolyl)-4-morpholinebutyrate as cream colored crystals, m.p. 96° -97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112095
Source datasetuspto-grants-1978_09
ORD IDord-556ce4f2e1c741ada993ba0bfd9ca199
Source noteuspto-grants-1978_09