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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255508Generated: October 29, 2026

Ethylamine → HCID 17875048, compound

https://huagongshe.com/reaction/2255508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 19737951HCID 19737951—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17875048HCID 1787504853.3%

Reaction Conditions

Temperature-16 °C

Reaction Steps

The product from Step C (1 g, 3 mmol) was dissolved in tetrahydrofuran (50 mL) containing triethylamine (1.7 mL, 12.0 mmol) and the solution was cooled to -16° C. Tosyl chloride (1.1 g, 6.0 mmol) was added and the mixture stirred for 18 h at room temperature after which time it was cooled to 0° C. and ethylamine (10 mL) was added. After heating at reflux for 1 h the solvent was evaporated and the residue dissolved in ethyl acetate (50 mL) and washed with 1N HCL (3×20 mL). The combined aqueous washes were basified (sodium bicarbonate) and extracted with ethyl acetate. The combined extracts were washed with saturated sodium bicarbonate solution (3×15 mL) and brine (3×15 mL), dried (MgSO4) and evaporated to give the desired free base (620 mg) as a syrup. This material was dissolved in ethanol (5 mL) and IN ethanolic HCL (5 mL) was added. This solution was then concentrated to dryness to give the desired product as a light yellow solid (400 mg): mp 243°-245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240923
Source datasetuspto-grants-1993_08
ORD IDord-0e16061764734d6ca7589782b0d8b483
Source noteuspto-grants-1993_08