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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Tetralone | HCID 10724 | — |
| Reactant | 5-Amino-3,4-dihydronaphthalen-1(2H)-one | HCID 11506505 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Amino-3,4-dihydronaphthalen-1(2H)-one | HCID 11506505 | — |
| Product | 5-CHLORO-1-TETRALONE | HCID 12206522 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132419B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-1010c3de09b24b38a22df62ec716b90a |
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| Source note | uspto-grants-2006_11 |
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