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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502300Generated: October 31, 2026

Dichloromethane → 1-(5-Amino-2-chloropyridin-4-yl)ethanol

https://huagongshe.com/reaction/1502300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl N-[6-chloro-4-(1-hydroxyethyl)-3-pyridyl]carbamateHCID 86674943—
Product1-(5-Amino-2-chloropyridin-4-yl)ethanolHCID 8667494487.3%

Reaction Steps

To a solution of tert-butyl 6-chloro-4-(1-hydroxyethyl)pyridin-3-ylcarbamate (823 mg, 3.02 mmol) in methylene chloride (40 mL, 500 mmol) was added trifluoroacetic acid (2 mL, 20 mmol). The reaction mixture was stirred at room temperature for 5 hours and then evaporated in vacuo. The resulting residue was dissolved in dichloromethane and washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4 and evaporated in vacuo to yield 455.2 mg (87%) of 1-(5-amino-2-chloropyridin-4-yl)ethanol which was carried forward without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-6371c1f45b90406dad3d66f23e19997d
Source noteuspto-grants-2015_12