HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176598Generated: November 1, 2026
Sulfuric Acid → Methyl 2-oxo-2,3,4,5-tetrahydro-1H-benz[b]azepine-9-carboxylate
https://huagongshe.com/reaction/1176598
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate | HCID 10867421 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 2-oxo-2,3,4,5-tetrahydro-1H-benz[b]azepine-9-carboxylate | HCID 68497596 | — |
Reaction Steps
Conc. H2SO4 is added dropwise at 0° C. to a solution of 3.040 g of methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate in 550 ml of chloroform, in the course of which the temperature is kept at 0-3° C. On completion of addition, the reaction solution is warmed to 10° C. and 21.80 g of sodium azide are added in portions over the course of 45 minutes. The reaction mixture is subsequently stirred at 50° C. over 2.5 hours. The reaction mixture is cooled to room temperature and subsequently poured onto a mixture of 200 g of potassium carbonate, 1000 ml of water and 400 g of ice. The mixture is made basic with 44 ml of 50% KOH and extracted with 2×500 ml of dichloromethane. The combined organic phases are washed with 1000 ml of water and concentrated. The title compound is obtained as a reddish solid from the residue by means of flash chromatography (SiO2 60F). Rf=0.25 (1:1 EtOAc-heptane); Rt=3.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842688B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-7b5aca8133324ce78775c482da2f902c |
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| Source note | uspto-grants-2010_11 |
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