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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75936Generated: October 26, 2026

1,4-Dioxane hydrochloride → (S)-1-(5-Fluoropyridin-2-yl)ethanamine

https://huagongshe.com/reaction/75936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant(S)-tert-Butyl (1-(5-fluoropyridin-2-yl)ethyl)carbamateHCID 71299175—
SolventDichloromethaneHCID 6344—
Product(S)-1-(5-Fluoropyridin-2-yl)ethanamineHCID 1609753198%

Reaction Steps

To the solution of (S)-tert-butyl-1-(5-fluoropyridin-2-yl)ethylcarbamate (Method 34, 12.8 g, 53.3 mmol) in DCM (100 ml) was added HCl/dioxane solution (107 ml, 4 N, 428 mmol). The reaction was stirred at room temperature for 3 hours. The solvent was removed and 50 ml of saturated sodium bicarbonate was added. The resulting aqueous solution was extracted with ether (6×400 ml), dried over sodium sulfate and concentrated to give the title compound (7.30 g, 98%) as pale yellow oil. 1H NMR (400 MHz) δ 8.44 (d, J=2.8 Hz, 1H), 7.66 (m, 1H), 7.53 (m, 1H), 4.01 (q, J=6.8 Hz, 1H), 1.94 (b, 2H), 1.26 (d, J=6.8 Hz, 3H). MS: Calcd.: 140. Found: [M+H]+ 141.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835465B2
Source datasetuspto-grants-2014_09
ORD IDord-81a91c37c2e04b3f8b8954ae840ce879
Source noteuspto-grants-2014_09