Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583403Generated: November 2, 2026

4-[(Pyridin-4-yl)sulfanyl]butanenitrile → 4-[(Pyridin-4-yl)sulfanyl]butan-1-amine

https://huagongshe.com/reaction/1583403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(Pyridin-4-yl)sulfanyl]butanenitrileHCID 13557536—
SolventBoraneHCID 6331—
SolventTetrahydrofuranHCID 8028—
Product4-[(Pyridin-4-yl)sulfanyl]butan-1-amineHCID 1355753786%

Reaction Steps

A solution of 14.35 g of 4-(4-pyridylthio)butanenitrile in 280 ml of 1 Molar borane in tetrahydrofuran was stirred over night at room temperature. The excess reagent was quenched by the careful addition of 100 ml of methanol. The reaction mixture was evaporated to dryness, diluted with 200 ml of methanol, evaporated, diluted with 100 ml of 6N hydrochloric acid and allowed to stand at room temperature for 72 hours. The resulting mixture was made strongly basic with 50% sodium hydroxide and was extracted with 4×150 ml of dichloromethane. The combined organic layers were dried over potassium carbonate, evaporated, and the residue was distilled to give 12.62 g (86%) of 4-(4-pyridylthio)butanamine, bp 180° C./0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551460
Source datasetuspto-grants-1985_11
ORD IDord-b7124c77736b40569a308c9b3fbcc8a2
Source noteuspto-grants-1985_11