Hydrochloric Acid → 5,6-Bis(acetoxy)-1-aminomethyl-3-phenyl-3,4-dihydronaphthalene hydrochloride

HRID 1089012노트

반응식

HRID 1089012 반응식
[ClH:1].[NH2:2][CH2:3][C:4]1[C:13]2[C:8](=[C:9]([OH:15])[C:10]([OH:14])=[CH:11][CH:12]=2)[CH2:7][CH:6]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:5]=1.Cl.C([O:25][CH2:26][CH3:27])C.[C:28](OC(=O)C)(=[O:30])[CH3:29]>>[ClH:1].[NH2:2][CH2:3][C:4]1[C:13]2[C:8](=[C:9]([O:15][C:26](=[O:25])[CH3:27])[C:10]([O:14][C:28](=[O:30])[CH3:29])=[CH:11][CH:12]=2)[CH2:7][CH:6]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:5]=1

참가 물질

5

실험 절차

A suspension of 7.6 g (25 mmol) of 1-aminomethyl-3,4-dihydro-5,6-dihydroxy-3-phenyl-naphthalene hydrochloride (Example 2B) in 400 mL of acetic anhydride saturated with anhydrous hydrogen chloride was stirred at ambient temperature for 48 h. Diethyl ether (approximately 2 L) was added and a solid was collected by filtration and washed with diethyl ether. Crystallization of the crude material (6.7 q) was achieved by dissolving the powder in 400 mL of hot ethanol, adding 100 mL of water, filtering the solution hot and allowing it to cool. The white crystals which formed were filtered and dried to give 2.8 g (29% yield) of 1-aminomethyl-5,6-bis(acetoxy)-3,4-dihydro-3-phenyl-naphthalene hydrochloride, m.p. 207°-208° C. 1H NMR (d6DMSO) delta 2.28 (s, 6H), 2.62 (dd, 1H), 2.95 (dd, 1H), 3.7-3.8 (m, 1H), 3.97 (s, 2H), 6.25 (d, 1H), 7.19 (d, 1H), 7.2-7.4 (m, 6H), 8.41 (br s, 3H).

후처리

  1. filtrationa solid was collected by filtration
  2. washwashed with diethyl ether
  3. customCrystallization of the crude material (6.7 q)
  4. dissolutionby dissolving the powder in 400 mL of hot ethanol
  5. additionadding 100 mL of water
  6. filtrationfiltering the solution hot
  7. temperatureto cool
  8. customThe white crystals which formed
  9. filtrationwere filtered
  10. customdried

출처 및 근거

ORD 기록
ord-058203e6ba7f4c8a8ace85c04d5e8ea6
출처 데이터셋
uspto-grants-1990_10
특허 번호
US04963568

반응 노트

불러오는 중…