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2-Methyl-2-butene → HCID 11482198, 화합물

HRID 1797488
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HRID 1797488 반응식
[CH:1]([C:3]1[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:7]([O:14][CH3:15])[C:6]([O:16][CH3:17])=[CH:5][CH:4]=1)=[O:2].P([O-])(O)(O)=[O:19].[Na+].CC(=CC)C.Cl([O-])=O.[Na+]>C(O)(C)(C)C.O1CCCC1.O>[CH2:12]([O:11][C:9]([C:8]1[C:7]([O:14][CH3:15])=[C:6]([O:16][CH3:17])[CH:5]=[CH:4][C:3]=1[C:1]([OH:19])=[O:2])=[O:10])[CH3:13]
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참가 물질

8

반응물 4

HCID 105532-Methyl-2-buteneHCID 610645Benzoic acid, 6-formyl-2,3-dimethoxy-, ethyl esterHCID 23668197Sodium ChloriteHCID 23672064Monosodium phosphate

생성물 1

HCID 11482198HCID 11482198, 화합물수율 80.7%

시약·촉매·용매 3

HCID 962Water용매
2회
HCID 6386tert-Butanol용매
HCID 8028Tetrahydrofuran용매

실험 절차

A solution of ethyl 6-formyl-2,3-dimethoxybenzoate (5.24 g, 22 mmol), sodium dihydrogen phosphate (3.60 g, 30 mmol) and 2-methyl-2-butene (10.3 ml, 96.8 mmol) in t-butanol (20 ml), tetrahydrofuran (20 ml) and water (20 ml) was stirred at room temperature for 10 min. To the obtained mixture was added sodium chlorite (6.76 g, 74.8 mmol) and the mixture was stirred at room temperature for 1 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to give 2-(ethoxycarbonyl)-3,4-dimethoxybenzoic acid (4.51 g, 80.7%) as crystals.

후처리

  1. extractionextracted with ethyl acetate
  2. washThe extract was washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was recrystallized from ethyl acetate-n-hexane

출처 및 근거

ORD 기록
ord-c60ced6484874ea2b4bef26ca3d679e4
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07034039B2

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