HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577500Generated: October 31, 2026
Sodium borohydride → 5,8-dichloro-3,4-dihydroisoquinolin-1(2H)-one
https://huagongshe.com/reaction/577500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 3,6-dichloro-2-(cyanomethyl)benzoate | HCID 86723725 | — |
| Catalyst | Dichlorocobalt hexahydrate | HCID 517166 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5,8-dichloro-3,4-dihydroisoquinolin-1(2H)-one | HCID 86723726 | 39% |
Reaction Steps
Cobalt (II) chloride hexahydrate (166 g, 0.70 mol) was added to a room temperature solution of ethyl 3,6-dichloro-2-(cyanomethyl)benzoate (253d, 90 g, 0.35 mol) in ethanol (1.5 L), and the resulting mixture cooled to 0° C. Sodium borohydride (66.3 g, 1.74 mol) was added in portions. The mixture was stirred at room temperature for 1 hour, and then refluxed overnight. The resulting suspension was filtered and the filtrate concentrated in vacuo. The solids in the filter cake were stirred in ethyl acetate (600 mL), and then filtered again. This procedure was repeated a second time. The combined filtrates were added to the original filtrate residue, and this organic solution washed with water (800 mL) and saturated aqueous sodium chloride solution (800 mL), dried over sodium sulfate, and concentrated in vacuo to give 5,8-dichloro-3,4-dihydroisoquinolin-1(2H)-one (253e, 29.3 g, 39% yield) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040515B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-b560f9e8d4ec4b52ae736f60d3f32e92 |
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| Source note | uspto-grants-2015_05 |
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