(R)-1-Phenylpropylamine → (R)-chroman-2-carboxylic acid

HRID 1752278

반응식

HRID 1752278 반응식
C1([C@H](N)CC)C=CC=CC=1.[O:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][CH2:13][C@@H:12]1[C:21]([O-:23])=[O:22].C1([C@H]([NH3+])CC)C=CC=CC=1>C(#N)C.C(OC)(C)(C)C>[O:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][CH2:13][C@@H:12]1[C:21]([OH:23])=[O:22]

참가 물질

5

실험 절차

To a solution of Intermediate-1 (18.6 g, 104 mmol) in acetonitrile (91 mL), (R)-(+)-1-phenylpropylamine (9.14 g, 67.9 mmol) in methyl tert butyl ether (MTBE) (12 mL) solution was added in dropwise manner. After about half of the total amount of the (R)-(+)-1-phenylpropylamine solution was added. The reaction mixture was seeded with few crystals of ((R)-(+)-1-phenyl propyl ammonium (R)-(−)-chromane-2-carboxylate). The resultant thick slurry was diluted with MTBE (80 mL) and the mixture was further stirred for 6 h at RT. The salt was filtered, washed with MTBE and dried. The salt (13.7 g) was suspended in MTBE (80 mL) further aqueous HCl solution (1:1) (88 mL) was added and the mixture was stirred in cooling to 0° C. The aqueous layer was extracted with methyl tert-butyl ether (70 mL×2). The extracts were combined with organic layer and the solution was washed with 1:1 HCl solution (40 mL). The organic layer was dried over Na2SO4 and evaporated under reduced pressure to afford the title compound as a white crystalline solid (6.5 g); m/z-178.02.

후처리

  1. filtrationThe salt was filtered
  2. washwashed with MTBE
  3. customdried
  4. additionwas added
  5. stirringthe mixture was stirred
  6. temperaturein cooling to 0° C
  7. extractionThe aqueous layer was extracted with methyl tert-butyl ether (70 mL×2)
  8. washthe solution was washed with 1:1 HCl solution (40 mL)
  9. dry with materialThe organic layer was dried over Na2SO4
  10. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-e77e936cf70144a08a87af15ed098aee
출처 데이터셋
uspto-grants-2015_10
특허 번호
US09163001B2

연결된 노트

불러오는 중…