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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628233Generated: October 25, 2026

Hydrochloric Acid → 1-(Thiazol-4-yl)cyclopropanamine

https://huagongshe.com/reaction/1628233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium HydroxideHCID 14798—
Reactant4-CyanothiazoleHCID 15069—
ReactantHCID 178418443HCID 178418443—
CatalystTitanium isopropoxideHCID 11026—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product1-(Thiazol-4-yl)cyclopropanamineHCID 5528567649.3%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Thiazole-4-carbonitrile (1035 mg, 9397 μmol) was azeotroped with toluene. Et2O was added, and the clear solution was cooled to −70° C., followed by addition of titanium tetraisopropoxide (3025 μl, 10337 μmol), and ethylmagnesium bromide (6265 μl, 18795 μmol). The reaction mixture turned yellow. It remained yellow until about 15 min. The reaction was raised to RT, the solution changed into black. After 1 h., boron trifluoride diethyl etherate (2361 μl, 18795 μmol) was added and stirred for 1.5 hr. Then 1N HCl 27 mL was added, followed by 100 mL ether, 95 mL 10% NaOH. The reaction was extracted with Et2O×2 and 30% IPA/CHCl3×1. The organic layer was concentrated and purified with silica gel chromatography using 0-10% MeOH/DCM. 650 mg of product 14.2.B was obtained in 49% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785468B2
Source datasetuspto-grants-2014_07
ORD IDord-ae043e8723ad458a9b60ddee57e3eb51
Source noteuspto-grants-2014_07