Trifluoroacetic acid → 2-Phenyl-2-o-tolylethanamine

Potassium tert-butoxyde (8.64 g, 77 mmol) was added, in one portion, to a cold (0° C.) solution of Tosmic (6.04 g, 27.8 mmol) in DMSO (15 mL) and stirred for 5 min. MeOH (0.2 mL) was then added followed by phenyl(o-tolyl)methanone (1.82 g, 9.2 mmol) in one portion. The reaction was warmed up slowly over 12 hours to room temperature. The reaction mixture was partitioned between saturated aqueous sodium carbonate and ethyl acetate. The organic phase was dried over sodium sulfate and evaporated under reduced pressure to give a residue. TFA (3.85 mL, 50 mmol) in THF (5 mL) was slowly added to a cool (0° C.) suspension of sodium borohydride (2.1 g, 50 mmol) in THF (5 mL) over 10 minutes. To this solution was added the residue dissolved in THF (5 mL) over 5 minutes. The resulting mixture was warmed to room temperature and stirred 16 hrs. The reaction mixture was partitioned between saturated aqueous sodium carbonate and ethyl acetate. The organic phase was dried over sodium sulfate and evaporated under reduced pressure and dissolved in methanol. This solution was then passed through SCX resin (12 g, 0.78 mmol/g) and washed with methanol. These washes were discarded and the cartridge treated with 2M ammonia in methanol. The ammonia solution was then evaporated to generate the desired compound (1.322 g, 63%). 1H NMR (400 MHz, DMSO-d6) δ ppm: 2.22 (3H, s) 3.04-3.16 (2H, m) 4.13 (1H, t, J=7.45 Hz) 7.08-7.31 (11H, m).

1. temperatureThe reaction was warmed up slowly over 12 hours to room temperature
2. customThe reaction mixture was partitioned between saturated aqueous sodium carbonate and ethyl acetate
3. dry with materialThe organic phase was dried over sodium sulfate
4. customevaporated under reduced pressure
5. customto give a residue
6. temperaturea cool
7. additionTo this solution was added the residue
8. stirringstirred 16 hrs
9. customThe reaction mixture was partitioned between saturated aqueous sodium carbonate and ethyl acetate
10. dry with materialThe organic phase was dried over sodium sulfate
11. customevaporated under reduced pressure
12. dissolutiondissolved in methanol
13. washwashed with methanol
14. additionthe cartridge treated with 2M ammonia in methanol
15. customThe ammonia solution was then evaporated

ORDレコード

ord-b95f3c766e2d4a89bb1457c8b50fc674

出典データセット

uspto-grants-2012_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08148400B2