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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020334Generated: November 1, 2026

Potassium tert-butoxide → HCID 58598878, compound

https://huagongshe.com/reaction/1020334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Benzyl-5-methoxy-2,3,3a,8a-tetrahydro-1H-2-aza-cyclopenta[a]inden-8-oneHCID 67203458—
CatalystPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
SolventDiethyl EtherHCID 3283—
ProductHCID 58598878HCID 58598878—

Reaction Steps

Ethyltriphenylphosphonium bromide (0.6 g, 1.6 mmol) and potassium tert-butoxide (0.18 g, 1.6 mmol) were added to a solution of 2-benzyl-5-methoxy-2,3,3a,8a-tetrahydro-1H-2-aza-cyclopenta[a]inden-8-one (from Example 1, Step C) (0.32 g, 1.1 mmol) in anhydrous ether (2.2 mL). The reaction mixture was stirred for 1 hour at room temperature then filtered through celite. The celite was washed with ether (10 mL), and the filtrate was concentrated. The crude product was purified by column chromatography (SiO2) using a 0-35% EtOAc-hexanes gradient to afford the subtitle compound in quantitative yield. MS calculated for C21H23NO+H: 306, observed: 306.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716324B2
Source datasetuspto-grants-2014_05
ORD IDord-e7472ef5927249c9888ba2eb559c454d
Source noteuspto-grants-2014_05