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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303330Generated: October 31, 2026

1,2-Dichloroethane → HCID 178420189, compound

https://huagongshe.com/reaction/2303330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant338733-58-7HCID 18461105—
ReactantHCID 178520508HCID 178520508—
SolventChloroformHCID 6212—
SolventSodium CarbonateHCID 10340—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 178420189HCID 178420189130.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432976B1
Source datasetuspto-grants-2002_08
ORD IDord-803556e40d5647d1820ec53668b0388a
Source noteuspto-grants-2002_08