HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851242Generated: October 31, 2026
Magnesium Chloride → HCID 12859196, compound
https://huagongshe.com/reaction/851242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | (S)-(+)-2-(Anilinomethyl)pyrrolidine | HCID 6950385 | — |
| Reactant | HCID 12859191 | HCID 12859191 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12859196 | HCID 12859196 | 28% |
Reaction Steps
2-Carbomethoxy-3-phenyl-1,3-diazabicyclo[3,3,0]octane prepared from 1.76 g of (S)-2-(anilinomethyl)pyrrolidine, as described in Example 8, was dissolved in 50 ml of THF, then admixed with 1.05 g of anhydrous magnesium chloride and refluxed by heating for 10 minutes. To the mixture cooled to -70° C., was added dropwise an ether solution containing 1.46 equivalents of ethylmagnesium bromide. The resulting mixture was treated as described in Example 12 to obtain 694 mg (28%) of 2-propionyl-3-phenyl-1,3-diazabicyclo[3,3,0]octane. NMR peaks: δ(ppm)=1.0 (3H, triplet), 1.4-2.1 (4H, multiplet), 2.1-2.6 (2H, multiplet), 2.6-3.3 (3H, multiplet), 3.5-3.9 (2H, multiplet), 4.2 (1H, singlet), 6.1-7.1 (5H, multiplet).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04383122 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-af121c8826bf4986bf7d8a24e0afed28 |
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| Source note | uspto-grants-1983_05 |
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