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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186811Generated: November 1, 2026

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

https://huagongshe.com/reaction/2186811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantBoron trifluoride etherateHCID 8000—
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 stirred solution of chloroacetonitrile (40 mL) and boron trifluoride etherate (20 mL, 0.16 mmol) at 0° C. was added 1-diazo-3,3-dimethyl-2-butanone in chloroacetonitrile (40 mL) dropwise over a period of 20 minutes. After addition was complete, the mixture was stirred at 0° C. for one hour and then partitioned between saturated NaHCO3 solution (700 mL) and CH2Cl2 (500 mL). The aqueous solution was. extracted with CH2Cl2 (500 mL) and the combined organic layers were washed with brine (400 mL) and dried over MgSO4. After filtration, the solution was concentrated and then distilled under vacuum using an oil bath temperature of 40° C. The 2-(chloromethyl)-5-t-butyloxazole (9.2 g, 44% overall from the acid chloride, C8H12CINO, MS m/e 174 (M+H)+) was obtained as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407124B1
Source datasetuspto-grants-2002_06
ORD IDord-5c0e8da4bfbc495482a6ba9a2875f6ab
Source noteuspto-grants-2002_06