HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156977Generated: October 31, 2026
Magnesium Chloride → HCID 12859198, compound
https://huagongshe.com/reaction/1156977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | (S)-(+)-2-(Anilinomethyl)pyrrolidine | HCID 6950385 | — |
| Reactant | HCID 12859191 | HCID 12859191 | — |
| Reactant | HCID 178418365 | HCID 178418365 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12859198 | HCID 12859198 | 79% |
Reaction Steps
2-Carbomethoxy-3-phenyl-1,3-diazabicyclo[3,3,0]octane prepared from 637 mg of (S)-2-(anilinomethyl)pyrrolidine was dissolved in 18 ml of THF, then admixed with 378 mg of anhydrous magnesium chloride, and refluxed for 10 minutes by heating. To the mixture cooled to -70° C., was added dropwise an ether solution containing 1.37 equivalents of isopropylmagnesium bromide. The resulting mixture was treated as in Example 12 to obtain 731 mg (79%) of 2-isobutyryl-3-phenyl-1,3-diazabicyclo[3,3,0]octane. NMR peaks: δ (ppm)=0.9 (3H, doublet), 1.1 (3H, doublet), 1.5-2.2 (4H, multiplet), 2.4-3.3 (4H, multiplet), 3.5-3.9 (2H, multiplet), 4.4 (1H, singlet), 6.2-7.1 (5H, multiplet).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04337346 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-401e211348264fc38d8570a909bb34aa |
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| Source note | uspto-grants-1982_06 |
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