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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576646Generated: October 26, 2026

Trifluoroacetic acid → 3-Bromo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine

https://huagongshe.com/reaction/576646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-Bromo-6-trityl-6,7-dihydro-5H-pyrrolo[3,4-b]pyridineHCID 57753674—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product3-Bromo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridineHCID 57753562—

Reaction Steps

To a cooled (0° C.) solution of 3-bromo-6-trityl-5,7-dihydropyrrolo[3,4-b]pyridine (1.57 g, 3.66 mmol) in chloroform (15 mL) and methanol (15 mL) was added trifluoroacetic acid (30 mL) over 1 min. On complete addition, the solution was stirred for 5 min then the cold bath removed and stirring continued for 30 min. This solution was concentrated under reduced pressure and the residue taken up in HCl (30 mL, 1M aq.). This mixture was extracted with ether (2×20 mL) then the aqueous phase basified with sodium hydroxide (5M aq.). This mixture was extracted with dichloromethane (3×20 mL). The combined dichloromethane extract was dried over magnesium sulfate and concentrated under reduced pressure to give the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040504B2
Source datasetuspto-grants-2015_05
ORD IDord-d2c6c0e000a54c1f8e8a26dbecadbd28
Source noteuspto-grants-2015_05