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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809137Generated: October 31, 2026

Hydrochloric Acid → HCID 57814299, compound

https://huagongshe.com/reaction/1809137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 57814296HCID 57814296—
ReactantHCID 66925267HCID 66925267—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57814299HCID 5781429961.1%

Reaction Steps

A mixture of (8) (81% pure, 3.82 g, 10.6 mmol) and (9) in THF (30 mL) was added triphenylphosphine (2.86 g, 10.9 mmol) at room temperature. After the solution was stirred for 15 minutes, potassium hydroxide (0.61 g, 10.9 mmol) in water (6 mL) was added. The resulting mixture was stirred at room temperature overnight. The mixture was acidified to pH˜3 with HCl (2M). The aqueous layer was washed numerous times with diethyl ether, and basified to pH>7 with NaOH (2M). The basic layer was extracted with ethyl acetate. The pooled organic layer was dried over magnesium sulfate. The mixture was filtered. Silica gel was added to the filtrate, and the solvent was removed under vacuum. Purification by chromatography on silica gel (2 to 10% methanol in dichloromethane) gave 1-(2,3-dichlorophenyl)-2-(pyridin-4-yl)ethanamine (10) as a solid (1.71 g, 6.48 mmol, 60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362022B2
Source datasetuspto-grants-2013_01
ORD IDord-8d1b60b1c59b4134bb3f2020c2ca0bc7
Source noteuspto-grants-2013_01