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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65837Generated: October 26, 2026

Benzene → 3-Benzylamino-1-indanol

https://huagongshe.com/reaction/65837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBenzylamineHCID 7504—
Reactant1,3-IndandioneHCID 11815—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Benzylamino-1-indanolHCID 22756094—

Reaction Steps

Stir indan-1,3-dione (7.31 g.), benzene (200 ml.) and benzylamine (5.90 g.) and reflux into a water separator for 6 hours. Cool, filter, and wash the dark solid with ether. Boil the solid with methylene chloride, filter and remove the solvent by boiling and replace with ether. Filter to get 4.51 g. of dark solid. Stir 4.30 g. of this solid with methanol (150 ml.) and add sodium borohydride (12.0 g.) portionwise with stirring over 4 hours. Let the reaction stand at room temperature then evaporate the solvent in vacuo and digest the residue with water and ether. Extract the mixture with ether and wash, dry and evaporate the solvent in vacuo. Recrystallize the residue from cyclohexane-ether to obtain 1.996 g. of the pure free base of the title compound, m.p. 121°-125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04129561
Source datasetuspto-grants-1978_12
ORD IDord-d5d463a177f34d02b1412d12bf02bce3
Source noteuspto-grants-1978_12