Trifluoroacetic acid → HCID 19925593, 화합물

HRID 2226171노트

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HRID 2226171 반응식
C(OC([NH:8][C:9]1[CH:10]=[C:11]([C:15]2([OH:21])[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[CH:12]=[CH:13][CH:14]=1)=O)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[NH2:8][C:9]1[CH:10]=[C:11]([C:15]2([OH:21])[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[CH:12]=[CH:13][CH:14]=1

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 19925596HCID 19925596, 화합물

생성물 1

HCID 19925593HCID 19925593, 화합물수율 77%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

To an ice-cooled solution of 4-(3-t-butyloxycarbonylaminophenyl)-4-hydroxytetrahydropyran (2.0 g, 6.8 mmol), prepared as in step 2, in dichloromethane (14 mL) was added trifluoroacetic acid (14, mL). The resulting solution was stirred for 0.25 hours at 0° C. and 1 hour at ambient temperature. The volatiles were removed in vacuo and the resulting solution was basified with saturated aqueous potassium carbonate. The resulting mixture was diluted with dichloromethane and the layers separated. The aqueous layer was extracted (4x, dichloromethane). The combined organic layers were dried (MgSO4), and concentrated in vacuo to provide a solid. Trituration with hexanes provided 4-(3-aminophenyl)-4-hydroxytetrahydropyran as a colorless solid (1.01 g, 77%). mp 154°-155° C. 1H NMR (300 MHz, CDCl13) δ7.17 (1H, dt, J=7.5 ,1 Hz), 6.84-6.88 (2H, m), 6.62 Hz), (1H, br d, J=7.5 Hz), 3.93 (2H, td, J=12, 12, 2.5 Hz), 3.84 (2H, ddd, J=12, 5, 1.5 2.05-32 (4H, m). MS m/e 193 (M+NH4 -H2O)+, 211 (M+NH4)+.

후처리

  1. customThe volatiles were removed in vacuo
  2. additionThe resulting mixture was diluted with dichloromethane
  3. customthe layers separated
  4. extractionThe aqueous layer was extracted (4x, dichloromethane)
  5. dry with materialThe combined organic layers were dried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customto provide a solid

출처 및 근거

ORD 기록
ord-c5a2abcbc2ef42479af5fb4829663c34
출처 데이터셋
uspto-grants-1994_09
특허 번호
US05346914

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