HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443816Generated: October 26, 2026
Ammonia → 3-Methoxymethyl-5-nitroisoquinoline
https://huagongshe.com/reaction/443816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methoxymethylisoquinoline | HCID 20571808 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 3-Methoxymethyl-5-nitroisoquinoline | HCID 12874847 | — |
Reaction Steps
3-Methoxymethylisoquinoline (68.8 g) is dissovled in 95% sulphuric acid (density 1.83; 300 cc). The solution is cooled to 0° C. and a mixture of 70% nitric acid (density 1.42; 25 cc) and 95% sulphuric acid (density 1.83; 100 cc) is added dropwise in the course of 30 minutes so as not to exceed 10° C. Stirring is continued for 16 hours, whilst allowing the temperature to return to about 20° C. The mixture is then poured into a mixture of ice and water (2 liters), and an ammonia solution containing 20% of NH3 (density 0.9) is added, without exceeding 30° C., until a pH of about 10 is obtained. The resulting yellow solution is extracted with methylene chloride (4×400 cc). The organic extracts are combined, washed with water (2×50 cc), dried over magnesium sulphate and filtered and the filtrate is evaporated to dryness at 40° C. under reduced pressure (20 mm Hg). 3-Methoxymethyl-5-nitroisoquinoline (78 g), m.p. 91° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04261992 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-ed58369132dd47f99cb8d5e259deaadb |
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| Source note | uspto-grants-1981_04 |
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