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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430393Generated: November 3, 2026

Acetonitrile → HCID 68802901, compound

https://huagongshe.com/reaction/1430393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTert-Butyl nitriteHCID 10906—
Reactant4-Hexyl-1,3-thiazol-2-amineHCID 13934262—
ReactantChloroform hexaneHCID 21585165—
CatalystCupric ChlorideHCID 24014—
ProductHCID 68802901HCID 68802901—

Reaction Steps

To 200 mL of acetonitrile was added 9.7 mL (81 mmol) of t-butyl nitrite and 8.75 g (65.1 mmol) of copper(II) chloride, and 10 mL of acetonitrile containing 10.0 g (54.3 mmol) of 2-amino-4-hexylthiazole (Helvetica Chemica Acta XXXII, Fasciculus I, 35 (1949)) dissolved therein was added to this portion-wise while cooling with ice under an argon atmosphere and the temperature thereof was returned to room temperature and the mixture was stirred for 2 hours. Then, the resultant reaction mixed liquid was poured into 100 ml of chloroform/hexane mixed liquid, and the precipitate was removed by filtration. The filtrate was washed with 100 ml of a 20 wt % hydrochloric acid aqueous solution three times, then, extracted with chloroform. The resultant extraction liquid was dried over anhydrous magnesium sulfate, then, concentrated under reduced pressure, and purified by silica gel column chromatography (development solvent:chloroform/hexane=1/1 (volumetric ratio)), to obtain the intended 2-chloro-4-hexylthiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940856B2
Source datasetuspto-grants-2015_01
ORD IDord-77511e3214d9495aaaf6d80bf7691d60
Source noteuspto-grants-2015_01