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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712469Generated: October 30, 2026

1-Bromo-3-chloropropane → tert-butyl 2-(3-chloropropyl)hexahydro-1H-pyrrolo[3,4-c]pyridine-5(6H)-carboxylate

https://huagongshe.com/reaction/712469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl octahydro-5H-pyrrolo(3,4-c)pyridine-5-carboxylateHCID 19691292—
SolventAcetoneHCID 180—
Producttert-butyl 2-(3-chloropropyl)hexahydro-1H-pyrrolo[3,4-c]pyridine-5(6H)-carboxylateHCID 8672949435%

Reaction Steps

A mixture of tert-butyl hexahydro-1H-pyrrolo[3,4-c]pyridine-5(6H)-carboxylate (1.70 g), 1-bromo-3-chloropropane (1.70 mL) and K2CO3 (3.30 g) in acetone was heated to reflux for 10 h, then cooled to rt and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 20:1 (v/v) DCM/MeOH) to give the title compound as yellow oil (0.79 g, 35.00%), HPLC: 80.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 303.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181277B2
Source datasetuspto-grants-2015_11
ORD IDord-eca307c8eef94724ae4bb92af284970a
Source noteuspto-grants-2015_11