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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987984Generated: November 1, 2026

Iodoethane → HCID 68996667, compound

https://huagongshe.com/reaction/1987984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactanttert-Butyl (1R,3s,5S)-9-azabicyclo[3.3.1]nonan-3-ylcarbaMateHCID 45792693—
SolventDichloromethaneHCID 6344—
ProductHCID 68996667HCID 6899666745%

Reaction Steps

Ethyl iodide (50 μL, 0.63 mmol) was added to a solution of the amine from Step B (100 mg, 0.42 mmol) in methylene chloride (2 mL) at 0° C. The mixture was allowed to warm to room temperature and stirred for 30 h. The mixture was quenched with a saturated solution of sodium bicarbonate and extracted with methylene chloride. The combined organic layers were washed with brine, dried (Na2SO4), filtered and concentrated. The crude material was purified by column chromatography (silica gel, 90:9:1 ethyl acetate/methanol/concentrated ammonium hydroxide) to afford tert-butyl 9-ethyl-9-azabicyclo[3.3.1]nonan-3-ylcarbamate (50 mg, 45%) as a white solid: 1H NMR (500 MHz, CDCl3) δ 4.28 (br s, 1H), 3.99 (br s, 1H), 3.13-3.10 (m, 2H), 2.63 (q, J=7.0 Hz, 2H), 2.38-2.30 (m, 2H), 1.90-1.82 (m, 3H), 1.48-1.46 (m, 1H), 1.44 (s, 9H), 1.16-0.95 (m, 7H); MS (ESI+) m/z 269 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553846B2
Source datasetuspto-grants-2009_06
ORD IDord-1505dcd0c81d4106ad596aa85227a2ae
Source noteuspto-grants-2009_06