Hydrochloric Acid → HCID 12004108, compound

Hydrazine monohydrate (3.1 mL) was added to a stirred solution of (R)-2-(2-methyl-4,4,4-trifluorobutyl)-1H-isoindole-1,3(2H)-dione (17.1 g) in anhydrous ethanol (85 mL) was heated to reflux. After three hours' reflux, the solution was cooled; ethanol (40 mL) was added; and the solution was acidified to pH 1 by addition of concentrated hydrochloric acid and was filtered. The filtrate was evaporated, and the residue was purified by sublimation (bath temperature 170° C., at 6.6 Pa) to yield (R)-2-methyl-4,4,4-trifluorobutylamine hydrochloride as a white solid (9.89 g, 88%); mp 187°-191° C.; partial NMR (300 MHz, DMSO-d6 -D2) shake): 1.05 (d,3H,CH3), 2.06-2.36(m,2H,CF3CH2) 2.36-2.54(m,1H,CHCH3) 2.73(dd,1H,CH2N), 2.87(dd,1H,CH2N) 8.20(br s,2H,NH2).

1. temperaturewas heated to reflux
2. temperatureAfter three hours' reflux
3. temperaturethe solution was cooled
4. filtrationwas filtered
5. customThe filtrate was evaporated
6. customthe residue was purified by sublimation (bath temperature 170° C., at 6.6 Pa)

ORD record

ord-0cf3da992e544b8096411774515f69df

Source dataset

uspto-grants-1993_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05274118