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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742449Generated: October 29, 2026

1-Indanone → HCID 19047540, compound

https://huagongshe.com/reaction/742449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-BromofuranHCID 89164—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19047540HCID 19047540104%

Reaction Steps

To a solution of 2.7 mL (0.027 mol) of 10M n-butyllithium in hexane in 70 mL of ether cooled to -78° C. was added 4 g (0.027 mol) of 3-bromofuran and the mixture was stirred for 15 min. To the above cooled mixture was added 3.17 g (0.024 mol) of indanone in 10 mL of THF and the mixture was allowed to warm to room temperature, and then stirred for 20 min. To the mixture was added saturated ammonium chloride solution and the resulting mixture was extracted with ethyl acetate (3×100 mL), and the organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo to afford 5 g of crude 1-(3-furyl)-indan-1-ol, as an orange oil, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554620
Source datasetuspto-grants-1996_09
ORD IDord-33fc585ebb3c4d0fba59bd5c2a3f9fc5
Source noteuspto-grants-1996_09