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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223119Generated: October 25, 2026

1-Indanone → 1-Indanol

https://huagongshe.com/reaction/223119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product1-IndanolHCID 2281974.4%

Reaction Conditions

Temperature35 °C

Reaction Steps

20 g Indanone (obtained according to Example VIII) is added to a solution of 1.5 molequivalent NaAlH2 (OC2H4OCH3)2 in a mixture of benzene and ether in the course of which the temperature raises to 35° C. Then the reaction mixture is stirred during one hour, poured out into ice and extracted with ether. The solution in ether is washed with NaCl solution, dried and evaporated. The residue is distilled under diminished pressure yielding 15.1 g indanol. B.p. 115° C./1 mm Hg. The indanol is dissolved in 100 ml cyclohexane and during 30 min. gaseous HCl is introduced followed by N2 to remove the excess of HCl. The reaction mixture is evaporated and the residue is distilled under diminished pressure yielding 12.9 g indanyl chloride. B.p. 95° C./1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352748
Source datasetuspto-grants-1982_10
ORD IDord-228021af54c942849e9dbb71f37de912
Source noteuspto-grants-1982_10