HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811037Generated: October 30, 2026
Methanesulfonic Acid → 7-Bromo-3,4-dihydroisoquinolin-1(2H)-one
https://huagongshe.com/reaction/1811037
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-Indanone, 6-bromo- | HCID 139778 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-3,4-dihydroisoquinolin-1(2H)-one | HCID 25067330 | 61% |
Reaction Steps
Sodium azide (0.431 g, 6.63 mmol) was added slowly to a mixture of 6-bromo-2,3-dihydro-1H-inden-1-one (1 g, 4.74 mmol) and methanesulfonic acid (15 mL, 231 mmol) in DCM (30 mL) at 0° C. The mixture was stirred at rt for 15 hrs, then was carefully quenched with 1 M aqueous sodium hydroxide (50 mL). The aqueous layer was extracted with DCM (3×50 mL), and the combined organic layers were washed with water (20 mL) and brine (20 mL), dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 90:10 hexane-EtOAc to EtOAc) to give 7-bromo-3,4-dihydroisoquinolin-1(2H)-one as white solid (650 mg, 61%). 1H NMR (400 MHz, chloroform-d) δ 8.35 (1 H, br. s.), 7.08-7.17 (1 H, m), 6.98-7.06 (1 H, m), 6.95 (1 H, d, J=1.98 Hz), 2.93 (2 H, t, J=7.59 Hz), 2.49-2.68 (2 H, m). Mass spectrum m/z 226, 228 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-21f37c062d2047e5a3f618517212db3a |
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| Source note | uspto-grants-2013_01 |
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