Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65838Generated: October 25, 2026

Benzylamine → 3-Benzylamino-1-indanol

https://huagongshe.com/reaction/65838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant3-Bromo-1-indanoneHCID 11745912—
SolventDiethyl EtherHCID 3283—
Product3-Benzylamino-1-indanolHCID 22756094—

Reaction Steps

Cool a solution of benzylamine (3.22 g.) in dry ether (25 ml.) to below 0° C. With stirring under nitrogen add a cooled (below 0° C.) solution of 3-bromo-1-indanone (3.17 g.) in ether (25 ml.) dropwise over 1.5 hours. Store the reaction under nitrogen at -10° C. for one day. Quickly filter the cold solution and add it cold to a stirring solution of one molar borane in tetrahydrofuran (60 ml.) below 0° C. and under nitrogen. Stir the solution for 18 hours at room temperature. Carefully add a solution of water (3.24 ml.) in tetrahydrofuran (20 ml.) dropwise, followed by 8.0 ml. of 5M isopropanolic --HCl, and continue stirring overnight. Store the reaction at -10° C. overnight, then filter the precipitate through filter-aid. Extract the dry solid mixture with methanol-methylene chloride, filter and evaporate the solvents in vacuo. Triturate the resulting solid with cold ethyl acetate, filter and dry to obtain 2.36 g. of the title product as the hydrochloride salt, m.p. 233-235°. λmaxKBr 3.0 μ (OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04129561
Source datasetuspto-grants-1978_12
ORD IDord-d1550dc8f84e476d99984a492aceb7c5
Source noteuspto-grants-1978_12