HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060249Generated: October 31, 2026
Chloroacetonitrile → 5-tert-Butyl-2-(chloromethyl)-1,3-oxazole
https://huagongshe.com/reaction/1060249
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Diazonio-3,3-dimethylbut-1-en-2-olate | HCID 21792784 | — |
| Product | 5-tert-Butyl-2-(chloromethyl)-1,3-oxazole | HCID 12968974 | — |
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 silica, 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521759B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-bfb6d5cf150d40dca186ab0913abc78f |
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| Source note | uspto-grants-2003_02 |
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