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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843247Generated: October 31, 2026

Ammonium Chloride → HCID 22617023, compound

https://huagongshe.com/reaction/843247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
ReactantHCID 11073627HCID 11073627—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22617023HCID 2261702365.3%

Reaction Steps

766 mg (5 mmol) of 4-cyclobutyl-2-methylthiazole was dissolved in 15 ml of anhydrous tetrahydrofuran and mixed with 561 mg (5 mmol) of potassium tert-butoxide, and 3 ml (5 mmol) of n-butyllithium (1.68M hexane solution) was added dropwise at −78° C. After 3 hours of stirring at the same temperature, 1270 mg (6 mmol) of 3-bromomethylbenzonitrile in 3 ml anhydrous tetrahydrofuran was added dropwise, and the reaction solution was stirred for one hour and 40 minutes. After addition of saturated aqueous ammonium chloride, the reaction solution was extracted with diethyl ether twice, and the organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=4:1) to give 876 mg of the title compound as a yellow oily substance in a yield of 64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376671B1
Source datasetuspto-grants-2002_04
ORD IDord-155388ce7550418c8d5fae6ed155d39a
Source noteuspto-grants-2002_04