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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790480Generated: November 2, 2026

6-Methoxy-1-Indanone → HCID 12374669, compound

https://huagongshe.com/reaction/1790480

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-1-IndanoneHCID 334036—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 12374669HCID 12374669100.7%

Reaction Steps

6-Methoxyindan-1-one (5.0 g) was dissolved in methanol (50 ml). Next, sodium tetrahydroborate (1.41 g) was added thereto at 0° C., and the resultant mixture was reacted at room temperature for 5 hr. The reaction solution was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with water, dried and concentrated under reduced pressure to give 6-methoxyindan-1-ol (5.1 g) as an oil. This alcohol was not purified but reacted as such with thionyl chloride (4.5 ml) in ether at room temperature for 6 hr. The reaction solution was poured into ice water and extracted with ether. The ether layer was washed with water, dried and concentrated under reduced pressure to give the title compound (2.76 g). (251-2) 1-(4-Acetylpiperazin-1-yl)-6-methoxyindan

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-5560cc829e98483ca2ad1691a83b6d91
Source noteuspto-grants-2006_07