Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621167Generated: November 1, 2026

2-Indanone → HCID 13132281, compound

https://huagongshe.com/reaction/621167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IndanoneHCID 11983—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 13132281HCID 1313228143.8%

Reaction Steps

In a solution of 13 g of 2-indanone in 100 ml of methanol, there is dissolved 13 g of β-alanine ethyl ester hydrochloride, and, with ice cooling and stirring, 6.5 g of sodium cyanoborohydride is added portionwise. After standing at room temperature overnight, the mixture is poured into 500 ml of ice water, made alkaline with sodium hydrogen carbonate and extracted with 200 ml of chloroform. The extract is washed with water, and dried, followed by distilling off chloroform under reduced pressure. To the residue, 10 ml of 20% ethanolic hydrochloric acid and 50 ml of ethyl ester are added successively, and the mixture is allowed to stand at room temperature. The resulting precipitate is collected by filtration and dried to give 10 g of N-(indan-2-yl)-β-alanine ethyl ester hydrochloride as colorless scales melting at 150°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822818
Source datasetuspto-grants-1989_04
ORD IDord-ce1ffa443df74c26a1d97970469bfa49
Source noteuspto-grants-1989_04