Hydrochloric Acid → HCID 22463777, 화합물
반응식
C([O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:13]=2)[CH:8]=[C:7]([C:21]([O:23][CH2:24]C)=[O:22])[CH:6]=1)(=O)C.[OH-].[Na+].Cl.OS(O)(=O)=O>O.C(O)C.CO.C([O-])(O)=O.[Na+]>[OH:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([N:15]3[CH2:20][CH2:19][O:18][CH2:17][CH2:16]3)[CH:13]=2)[CH:8]=[C:7]([C:21]([O:23][CH3:24])=[O:22])[CH:6]=1참가 물질
실험 절차
A solution of ethyl 4-acetoxy-6-morpholino-2-naphthoate (12.0 g, 34.9 mmol) and sodium hydroxide (8.4 g, 210 mmol) in water (200 cm3) and ethanol (40 cm3) was maintained at 80-90° C. for 3 hours. The cooled solution was poured into water (750 cm3) and cautiously neutralised with HCl (2M). The resulting suspension was extracted with EtOAc.(5×100 cm3). The combined extracts were dried (Na2SO4) and evaporated to give a brown solid. This solid was dissolved in methanol (200 cm3) containing c. H2SO4 (˜3 cm3) and was refluxed for 5 hours. The cooled mixture was diluted with water (900 cm3) and aq. sat. NaHCO3 solution (100 cm 3) then extracted with EtOAc (6×50 cm3). The combined extracts were washed with aq. sat. NaHCO3 (4×100 cm3) and water (100 cm3). Removal of the dried (Na2SO4) EtOAc gave a pale brown solid which was recrystallised from EtOAc/hexane to afford methyl 4-hydroxy-6-morpholino-2-naphthoate (yield=5.14 g, theoretical yield=10.0 g, 51.2%, m.p.=231-233.5° C. (uncorrected)).
후처리
- extractionThe resulting suspension was extracted with EtOAc
- dry with materialThe combined extracts were dried (Na2SO4)
- customevaporated
- customto give a brown solid
- additioncontaining c
- extractionthen extracted with EtOAc (6×50 cm3)
- washThe combined extracts were washed with aq. sat. NaHCO3 (4×100 cm3) and water (100 cm3)
- customRemoval of the
- dry with materialdried (Na2SO4) EtOAc
- customgave a pale brown solid which
- customwas recrystallised from EtOAc/hexane
출처 및 근거
- ORD 기록
- ord-d4e16269678c4895b472b6f5dbc64d12
- 출처 데이터셋
- uspto-grants-2001_06
- 특허 번호
- US06248264B1
반응 노트
불러오는 중…