HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303330Generated: October 31, 2026
1,2-Dichloroethane → HCID 178420189, compound
https://huagongshe.com/reaction/2303330
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 338733-58-7 | HCID 18461105 | — |
| Reactant | HCID 178520508 | HCID 178520508 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 178420189 | HCID 178420189 | 130.1% |
Reaction Steps
A mixture of 0.25 g of 3-benzyl-8-aza-bicyclo[3.2.1]octane, 0.45 g of 3-(1H-imidazol-4-yl)-propionaldehyde, 5 mL of 1,2-dichloroethane and 0.5 g of sodium triacetoxyborohydride was stirred at room temperature for 48 h. The reaction mixture was diluted with 50 mL chloroform and 10 mL saturated aqueous Na2CO3 and the layers separated. The aqueous layer was extracted with 2×25 mL of chloroform and the combined organic layers dried over magnesium sulfate and concentrated under reduced pressure. Purification by chromatography eluting with 90:10:1 CHCl3:MeOH:NH4OH gave 0.25 g of 3-benzyl-8-[3-(1H-imidazol-4-yl)-propyl]-8-aza-bicyclo[3.2.1]octane as a 2:1 mixture of exo:endo isomers. MS (m+1)=310.3; 1H NMR (400 MHz, CDCl3) 7.5-7.1 (complex, 6H), 6.75 (s, 1H), 3.22 (s, 2H), 2.75 (m, 2.6 H), 2.5 (d, 0.7×2H), 2.45 (m, 2H), 2.1 (m, 2H), 1.95 (m, 2H), 1.8 (m, 3H), 1.5 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432976B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-803556e40d5647d1820ec53668b0388a |
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| Source note | uspto-grants-2002_08 |
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