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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525363Generated: November 2, 2026

Ethyl Acetate → HCID 12885306, compound

https://huagongshe.com/reaction/525363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant(1-hydroxycyclohexyl)(phenyl)acetic acidHCID 226204—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 12885306HCID 1288530631%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a 100 mL round bottom flask charged with 2-(1-hydroxycyclohexyl)-2-phenylacetic acid (6.5 g, 28.14 mmole, 1 eq.) in toluene (100 mL) were added TEA (2.5 eq) and diphenyl phosphoryl azide (2 eq). The resulting mixture was then stirred at 120° C. for 12 hours. Reaction progress was monitored by TLC (TLC eluent: 30% EtOAc in hexane). The reaction mixture was then cooled and toluene was removed under reduced pressure to afford the product. The product thus obtained was purified by column chromatography using silica gel and eluting with 10% EtOAc in hexane to afford 4-phenyl-1-oxa-3-azaspiro[4.5]decan-2-one (2 g, 31%). 1H NMR (400 MHz, DMSO-d6) δ: 8.04 (s, 1H), 7.26-7.41 (m, 5H), 4.54 (s, 1H), 1.93-1.97 (m, 1H), 1.48-1.78 (m, 4H), 1.12-1.33 (m, 5H). m/z (ESI) 232.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340549B2
Source datasetuspto-grants-2016_05
ORD IDord-3a79d719e789438ca20d13cadd6fcac1
Source noteuspto-grants-2016_05