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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637242Generated: November 2, 2026

Chloroacetonitrile → 5-tert-Butyl-2-(chloromethyl)-1,3-oxazole

https://huagongshe.com/reaction/1637242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Diazonio-3,3-dimethylbut-1-en-2-olateHCID 21792784—
Product5-tert-Butyl-2-(chloromethyl)-1,3-oxazoleHCID 12968974—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2 mL (2.3 g, 16 mmol) of boron trifluoride etherate in 20 mL of chloroacetonitrile at 0° C. was added a solution of 1.33 g (10 mmol) of 1-diazo-3,3-dimethyl-2-butanone in 5 mL of chloroacetonitrile dropwise. The resulting solution was stirred at 0° C. for 0.5 h. The reaction mixture was added to saturated aqueous sodium bicarbonate solution to neutralize the acid and the product was extracted three times with dichloromethane. The combined extracts was dried (sodium sulfate), concentrated and purified by flash column chromatography (Merck silic a, 25×200 mm, dichloromethane) to give 1.1 g of 2-(chloromethyl)-5-t-butyloxazole as a yellow liquid (6.4 mmol, 64% overall from the acid chloride). 1H NMR δ (CDCl3): 1.30 (s, 9 H), 4.58 (s, 2 H), 6.68 (s, 1 H); MS 174 (M+H)+ ; TLC: Rf (silica gel, dichloromethane)=0.33;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040321
Source datasetuspto-grants-2000_03
ORD IDord-6f2935a5bbef4f7e98166bd61f753e15
Source noteuspto-grants-2000_03