HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243749Generated: October 28, 2026
Ammonium Chloride → HCID 86653809, compound
https://huagongshe.com/reaction/243749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Bromocyclopropane | HCID 78037 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Methyl 4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-acetate | HCID 13051081 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86653809 | HCID 86653809 | 79% |
Reaction Steps
An anhydrous THF (50 mL) solution of bromocyclopropane (8.3 mL) was added dropwise to a metal magnesium (2.5 g), while heating. After the termination of dropwise addition, an anhydrous THF (20 mL) was added thereto, and the mixture was refluxed under heating for an additional 2 hours. Thereafter, the reaction mixture was allowed to air-cool, and this solution was added dropwise to an anhydrous THF (30 mL) solution of methyl (4-oxo-4,10-dihydro-9-oxa-3-thiabenzo[f]azulen-6-yl)acetate (10.0 g) previously chilled in an ice bath. After stirring the mixture for 30 minutes, an aqueous saturated ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated sodium chloride solution, and thereafter dried over anhydrous sodium sulfate. The solvents were distilled off under a reduced pressure, and the residue obtained was purified by silica gel column chromatography (hexane-ethyl acetate=5:1), to give 9.0 g (79%) of the captioned compound as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653285B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-3aac4aea93524bc2a2e500c285891a92 |
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| Source note | uspto-grants-2014_02 |
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