Hydrochloric Acid → HCID 21506798, 화합물
반응식
[NH:1]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]2([C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10](=[O:17])[CH2:9][CH2:8]2)[C:2]1=[O:18].[H-].[Na+].S(OCC)(O[CH2:25][CH3:26])(=O)=O.Cl>CN(C)C=O>[CH2:25]([N:1]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]2([C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10](=[O:17])[CH2:9][CH2:8]2)[C:2]1=[O:18])[CH3:26]참가 물질
실험 절차
To 24.3 grams (0.1 M) of 2,3-dihydrospiro-[naphthalene-1(4H),3'-piperidine]-2',4,6'-trione in 300 milliliters of dry dimethylformamide maintained under nitrogen atmosphere was added with stirring 4.37 grams (0.1 M) of a 55 per cent suspension of sodium hydride in mineral oil. After stirring for five minutes, 16.0 grams (0.1 M) of diethyl sulfate were added in one portion. The slightly exothermic reaction mixture was allowed to stir for a short time and concentrated hydrochloric acid was added dropwise until the reaction mixture was slightly acidic. The reaction solvent was removed under reduced pressure at steam bath temperature and the resulting oil extracted into ether. The ether extracts were washed with 5 percent sodium hydroxide solution, water, and then dried (MgSO4). After filtration, the ether was removed, leaving a residue, which was recrystallized from diethyl ether to give 34.9 grams (64%) of 1'-ethyl-2,3-dihydrospiro-[naphthalene-1(4H),3'-piperidine]-2',4,6'-trione, melting point 85.5°-89° C.
후처리
- additionwas added
- additionwas added dropwise until the reaction mixture
- customThe reaction solvent was removed under reduced pressure at steam bath temperature
- extractionthe resulting oil extracted into ether
- washThe ether extracts were washed with 5 percent sodium hydroxide solution, water
- dry with materialdried (MgSO4)
- filtrationAfter filtration
- customthe ether was removed
- customleaving a residue, which
- customwas recrystallized from diethyl ether
출처 및 근거
- ORD 기록
- ord-9270429a0ab54c6992aa61be44f0ebcd
- 출처 데이터셋
- uspto-grants-1976_10
- 특허 번호
- US03985888
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