Hydrochloric Acid → (5-(Trifluoromethyl)-1,2-oxazol-3-yl)methanamine hydrochloride
Reaction equation
[F:1][C:2]([F:11])([F:10])[C:3]1[O:7][N:6]=[C:5]([CH2:8][NH2:9])[CH:4]=1.[ClH:12]>C(O)C.O1CCOCC1>[ClH:12].[F:11][C:2]([F:1])([F:10])[C:3]1[O:7][N:6]=[C:5]([CH2:8][NH2:9])[CH:4]=1Participants
5
Procedure
To a solution of (5-(trifluoromethyl)isoxazol-3-yl)methanamine in 25 ml ethanol was added under cooling 5.12 mL 4M−HCl solution in dioxane over a period of 10 min. The ice-bath was removed and 25 ml diethyl ether was added drop by drop. Precipitation. Filtered off and washed with diethyl ether 83×5 mL). Dried in vacuo at 40° C. to yield 2.65 g of the title compound as a white solid. MS (EI): 166 (M+H)+.
Workup
- customThe ice-bath was removed
- addition25 ml diethyl ether was added drop by drop
- customPrecipitation
- filtrationFiltered off
- washwashed with diethyl ether 83×5 mL)
- customDried in vacuo at 40° C.
Sources & evidence
- ORD record
- ord-5a1a1df029354abd9e935022c95169a6
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08729105B2
Reaction notes
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