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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839519Generated: October 29, 2026

Ammonium Acetate → 5,6-Dichloro-indan-1-ylamine

https://huagongshe.com/reaction/839519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5,6-Dichloro-2,3-dihydro-1H-inden-1-oneHCID 22903609—
Product5,6-Dichloro-indan-1-ylamineHCID 20323400—

Reaction Steps

Following the procedure of Example 1, 5,6-dichloro-1-indanone was reacted with ammonium acetate and sodium cyanoborohydride to yield 5,6-dichloro-1-aminoindane; yield = 670 mg. The crystalline compound was treated with 360 mg. of maleic acid in 25 ml. of isopropanol. The maleate salt crystallized and was separated by filtration. Recrystallization of the salt from a 1:3 isopropanol/ethyl acetate solvent mixture yielded 650 mg. of 5,6-dichloro-1-aminoindane maleate melting at 167°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04096173
Source datasetuspto-grants-1978_06
ORD IDord-ff672ca82f8f47aca19d173fbfa32228
Source noteuspto-grants-1978_06