Sodium Hydroxide → 6-Bromo-1,2-dihydrospiro(indole-3,4'-oxane)
반응식
[Br:1][C:2]1[CH:7]=[C:6]2[NH:8][C:9](=O)[C:10]3([CH2:15][CH2:14][O:13][CH2:12][CH2:11]3)[C:5]2=[CH:4][CH:3]=1.COCCO[AlH2-]OCCOC.[Na+].[OH-].[Na+]>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:7]=[C:6]2[NH:8][CH2:9][C:10]3([CH2:15][CH2:14][O:13][CH2:12][CH2:11]3)[C:5]2=[CH:4][CH:3]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
A heterogeneous mixture of 6-bromo-2′,3′,5′,6′-tetrahydrospiro[indoline-3,4′-pyran]-2-one (3.5 g, 12.4 mmol) in toluene (25 mL) was stirred at 80° C. To the heated mixture was added a solution of Red-Al (65% in toluene, 11.6 mL, 37.2 mmol) and the mixture was stirred at 80° C. for 50 min. After this time the mixture was cooled to 0° C. and quenched with a 2 N solution of aqueous NaOH (31 mL, 62 mmol). The mixture was extracted with EtOAc (2×100 mL). The combined extracts were washed with brine (3×100 mL), dried over Na2SO4, filtered, and evaporated in vacuo. The resulting residue was purified by column chromatography (0 to 100% gradient of DCM-MeOH—NH4OH (89:9:1) in DCM) to give 6-bromo-2′,3′,5′,6′-tetrahydrospiro[indoline-3,4′-pyran] as a yellow solid. Mass Spectrum (ESI) m/e 268 [(M+1) (79Br)] and 270 [(M+1) (81Br)].
후처리
- stirringthe mixture was stirred at 80° C. for 50 min
- temperatureAfter this time the mixture was cooled to 0° C.
- extractionThe mixture was extracted with EtOAc (2×100 mL)
- washThe combined extracts were washed with brine (3×100 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated in vacuo
- customThe resulting residue was purified by column chromatography (0 to 100% gradient of DCM-MeOH—NH4OH (89:9:1) in DCM)
출처 및 근거
- ORD 기록
- ord-00a2f7b57be749289876b640c887913a
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765940B2
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