HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837474Generated: October 31, 2026
HCID 12128809, compound → 2,5-Dibromo-3,4-dihydro-1(2H)-naphthalenone
https://huagongshe.com/reaction/1837474
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 12128809 | HCID 12128809 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,5-Dibromo-3,4-dihydro-1(2H)-naphthalenone | HCID 12128808 | 98.5% |
Reaction Steps
A clear yellow solution of 5-bromo-3,4-dihydro-1(2H)-Naphthalenone(12.09 g, 53.7 mmol) in freshly opened Et2O (220 mL) under an N2 atmosphere was chilled to −5° C. HCl was bubbled in subsurface for 1 min, causing no visible change. The dropwise addition of a solution of Br2 (8.58 g, 53.7 mmol) in CH2Cl2 (20 mL) and Et2O (2 mL) to the vigorously stirring solution of 5-bromo-3,4-dihydro-1(2H)-naphthalenone over 2 h (each drop was allowed to fully decolorize before adding the next) produced a product mixture that assayed by HPLC. Peak area showed 79.4% title compound, 9.5% unreacted 5-bromo-3,4-dihydro-1(2H)-naphthalenone, 0.6% unidentified, and 9.4% 2,2,5-tribromo-1-tetralone. The addition of H2O produced a top light brown organic phase, and a clear, colorless bottom aqueous phase which was separated. After drying with MgSO4, the organic layer was concentrated in vacuo at room temperature to give the crude intermediate title compound as a light brown oil (16.08 g, 98.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06784180B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-2b1fe5b4dc964e399f59066bede4a5b4 |
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| Source note | uspto-grants-2004_08 |
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