HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743695Generated: October 31, 2026
Sodium Iodide → 3-Allyl-8-benzyl-3,8-diazabicyclo[3.2.1]octane
https://huagongshe.com/reaction/1743695
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Cis-1-benzyl-2,5-bis(chloromethyl)pyrrolidine hydrochloride | HCID 22940372 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Allyl-8-benzyl-3,8-diazabicyclo[3.2.1]octane | HCID 22235589 | 98.7% |
Reaction Steps
Allylamine (9.5 mL, 0.13 mol) was added to a suspension of cis-1-benzyl-2,5-bis(chloromethyl)pyrrolidine hydrochloride (37.5 g, 0.13 mol, from step (e) above), NaI (47.6 g, 0.32 mol) and NaHCO3 (106.7 g, 1.27 mol) in acetonitrile (1.8 L). The reaction was heated at reflux for 8 h, filtered, and the filtrate concentrated in vacuo. The residue was partitioned between ethyl acetate and ice cold 1 N NaOH. The ethyl acetate layer was separated, dried (Na2SO4), filtered and concentrated in vacuo to afford 31.1 g of an oil. The oil was chromatographed on a column of silica (75 mm×220 mm) eluting with a mixture of chloroform, methanol and conc. NH4OH (240:9:1). Fractions (100 mL each) 5–10 were combined and concentrated in vacuo to afford 22.2 g (72%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012074B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-03e0cefb5d4c4905bea7fec2d9619c0b |
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| Source note | uspto-grants-2006_03 |
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