1,4-Dibromobutane → 1,1-Dimethylethyl 4-{4-[(4-bromobutyl)oxy]butyl}benzoate
반응식
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:8][CH:7]=1.[Br:19][CH2:20][CH2:21][CH2:22][CH2:23]Br.[OH-].[Na+]>S(=O)(=O)(O)[O-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[Br:19][CH2:20][CH2:21][CH2:22][CH2:23][O:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:14])([CH3:15])[CH3:16])=[O:11])=[CH:8][CH:7]=1참가 물질
실험 절차
To 1,1-dimethylethyl 4-(4-hydroxybutyl)benzoate (0.85 g, 3.4 mmol, e.g. which can be as prepared in Intermediate 23) was added 1,4-dibromobutane (1.22 ml, 10.2 mmol, 3 equivalents, commercially available e.g. from Aldrich), tetra-n-butylammonium bisulphate (0.034 g, 0.1 mmol, 0.03 equivalents) and aqueous sodium hydroxide solution (50% w/v NaOH, 5 ml). The resultant biphasic mixture was stirred at room temperature over the weekend (this can be e.g. about 64 hours), diluted with water (20 ml) and extracted with diethyl ether (50 ml). The organic extract washed with water (20 ml), dried (Na2SO4) and evaporated to dryness. The residue was purified by passing through a 50 g silica SPE cartridge eluting with cyclohexane (100 ml), 9:1 cyclochexane:ethyl acetate (100 ml), 4:1 cyclohexane:ethyl acetate (200 ml) and 1:1 cyclohexane:ethyl acetate (100 ml). The 4:1 cyclohexane:ethyl acetate fraction containing the product was evaporated to give the title compound (1.05 g). LCMS showed TRET=4.14 min with: MH+=385 (trace), and [MH]++18 adduct=402/404 (Bromine isotope pattern).
후처리
- custome.g. about 64 hours
- extractionextracted with diethyl ether (50 ml)
- extractionThe organic extract
- washwashed with water (20 ml)
- dry with materialdried (Na2SO4)
- customevaporated to dryness
- customThe residue was purified
- washeluting with cyclohexane (100 ml), 9:1 cyclochexane
- additionThe 4:1 cyclohexane:ethyl acetate fraction containing the product
- customwas evaporated
출처 및 근거
- ORD 기록
- ord-9bfdf8894ebe480a9e5b4cab8ce862be
- 출처 데이터셋
- uspto-grants-2011_08
- 특허 번호
- US08003663B2
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