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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712489Generated: October 29, 2026

Iodoethane → 6-benzyl-1-ethyloctahydro-1H-pyrrolo[3,4-b]pyridine

https://huagongshe.com/reaction/712489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant6-Benzyloctahydro-1H-pyrrolo[3,4-b]pyridineHCID 11356376—
SolventTetrahydrofuranHCID 8028—
Product6-benzyl-1-ethyloctahydro-1H-pyrrolo[3,4-b]pyridineHCID 8672949945.6%

Reaction Steps

To a solution of 6-benzyloctahydro-1H-pyrrolo[3,4-b]pyridine (5.00 g) in THF was added 80% NaH (3.00 g) at room temperature. The reaction mixture was stirred for 30 min, and 5.3 mL of iodoethane was added dropwise. The reaction mixture was stirred for another 5 h, and then quenched with ice-water. The resulted mixture was extracted with CH2Cl2 (70 mL×5). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was chromatographed with a silica gel column (eluting agent: 30:1 (v/v) DCM/MeOH) to give the title compound as a pale yellow solid (2.58 g, 45.60%). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 245.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181277B2
Source datasetuspto-grants-2015_11
ORD IDord-892c5dcd9c524bddb90de900dac7e0ce
Source noteuspto-grants-2015_11