HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895863Generated: October 31, 2026
Diphenylmethane → 6-methoxyisoquinolin-1(2H)-one
https://huagongshe.com/reaction/1895863
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diphenylmethane | HCID 7580 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-Propenoic acid, 3-(3-methoxyphenyl)- | HCID 87155 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-methoxyisoquinolin-1(2H)-one | HCID 21889854 | 33% |
Reaction Steps
Ethyl chloroformate (4.3 mL, 44.5 mmol) was added drop wise at 0° C. to a solution of 3-methoxy cinnamic acid (5.3 g, 29.7 mmol) and triethylamine (8.3 mL, 59.4 mmol) in acetone (35 mL). After 1 h at 0° C., aqueous sodium azide (3.1 g, 47.5 mmol, 16 mL water) was added drop wise and the reaction mixture was stirred at 23° C. for 16 h. Water (50 mL) was added to the mixture and the volatile was removed under vacuo. The resulting slurry was extracted with toluene (3×25 mL) and the combined organic layers were dried (MgSO4). The dried solution was filtered and added drop wise at 190° C. to a solution of diphenylmethane (25 mL) and tributylamine (14.2 mL, 59.4 mmol). The toluene was distilled off as added. After complete addition, the reaction temperature was raised to 210° C. for 2 h. After cooling, the precipitated product was collected by filtration and washed with hexanes and dried under vacuum to yield 6-Methoxy-2H-isoquinolin-1-one (1.7 g, 9.7 mmol, 33% yield). MS m/z 176 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518874B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a059590700164b7e9247d73e00c721d6 |
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| Source note | uspto-grants-2013_08 |
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