Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363115Generated: October 31, 2026

4-Hydroxy-1-indanone → HCID 67111152, compound

https://huagongshe.com/reaction/2363115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-1-indanoneHCID 590547—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
ProductHCID 67111152HCID 6711115217.1%

Reaction Steps

To a suspension of CH3CH2PPh3I (677 mg, 1.62 mmol) in Et2O (10 mL) was added t-BuOK (181 mg, 1.62 mmol). The mixture was stirred for 15 minutes, to which was added dropwise 4-hydroxy-indan-1-one (200 mg, 1.35 mmol). The mixture was stirred at room temperature overnight and then diluted with diethylether. The mixture was filtered on a pad of celite, and the filtrate was concentrated. The crude residue was purified by column chromatography to give 1-ethylidene-indan-4-ol (37 mg, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691855B2
Source datasetuspto-grants-2014_04
ORD IDord-84ffd0e65b794f49b55e3b44fbed8e79
Source noteuspto-grants-2014_04