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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244415Generated: November 2, 2026

Trifluoroacetic acid → HCID 58674938, compound

https://huagongshe.com/reaction/2244415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58674936HCID 58674936—
SolventDichloromethaneHCID 6344—
ProductHCID 58674938HCID 58674938102.2%

Reaction Steps

A solution of acetic acid 6-tert-butoxycarbonylamino-pyridin-2-ylmethyl ester (0.85 g, 3.18 mmol) in dichloromethane (30.00 ml) was cooled to 0° C. and trifluoroacetic acid (2.40 ml) was added dropwise. After stirring at room temperature for 3 h, further trifluoroacetic acid (1.50 ml) was added and stirring was maintained for further 2 h. The reaction mixture was basified with 1 N sodium bicarbonate (54.00 ml) to a pH 8. The organic phase was separated and the aqueous phase extracted twice with dichloromethane. The combined organic layers were dried over sodium sulphate and evaporated to yield pure acetic acid 6-amino-pyridin-2-ylmethyl ester (0.54 g, 100%) as a white solid, MS (ISP): m/e=167.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678815B2
Source datasetuspto-grants-2010_03
ORD IDord-6777902dc51947a28fc2c1cb3c6cba4d
Source noteuspto-grants-2010_03