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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719167Generated: October 30, 2026

Hydrochloric Acid → 5-Amino-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/719167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-TetraloneHCID 10724—
Reactant5-Amino-3,4-dihydronaphthalen-1(2H)-oneHCID 11506505—
ReactantSodium NitriteHCID 23668193—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
Product5-Amino-3,4-dihydronaphthalen-1(2H)-oneHCID 11506505—
Product5-CHLORO-1-TETRALONEHCID 12206522—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Amino-1-tetralone was prepared from α-tetralone according to the literature (J. Am. Chem. Soc. 1994, p4852). A mixture of 5-amino-1-tetralone (80 mg) and concentrated hydrochloric acid (1 mL) was cooled to 0° C. A solution of sodium nitrite (35 mg) in water (0.5 mL) was added dropwise to the stirring solution. The cold diazonium solution was then poured rapidly onto a stirring solution of copper (I) chloride (62 mg) in concentrated hydrochloric acid (1 mL). The reaction mixture was allowed to warn to ambient temperature and then stirred for 1.5 hours. The mixture was then extracted with ethyl acetate, washed with water, dried (MgSO4) and the solvent removed in vacuo to yield 5-chloro-1-tetralone as a brown solid (87 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132419B2
Source datasetuspto-grants-2006_11
ORD IDord-1010c3de09b24b38a22df62ec716b90a
Source noteuspto-grants-2006_11