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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421931Generated: November 3, 2026

Trifluoroacetic acid → HCID 63317696, compound

https://huagongshe.com/reaction/2421931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86629202HCID 86629202—
SolventDichloromethaneHCID 6344—
ProductHCID 63317696HCID 6331769684.8%

Reaction Steps

To a clear pale yellow mixture of the tert-butyl [2-(5-bromopyrimidin-2-yl)ethyl]carbamate (0.22 g, 0.7 mmol) in dichloromethane (2 ml) was added trifluoroacetic acid (10 equivs) and the mixture was left to stir at room temperature for 7 hrs and left to stand overnight. Saturated sodium bicarbonate solution was added until the effervescence stopped (to give a basic medium). The organic phase was collected, dried over MgSO4, and evaporated in vacuo after filtration, to yield to 0.12 g of 2-(5-bromopyrimidin-2-yl)ethanamine (80%) which is used directly without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960391B2
Source datasetuspto-grants-2011_06
ORD IDord-33d82b13775c41ab80f35d2b18deea5e
Source noteuspto-grants-2011_06