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Sodium Hydroxide → (E)-Methyl 3-chloro-2-(2-cyanovinyl)benzoate

HRID 84933
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HRID 84933 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4](=O)[O:5][C:6]2=[O:11].[H-].[C:14](O[Al](OC(C)(C)C)OC(C)(C)C)([CH3:17])(C)[CH3:15].[Li+].C1(P(=CC#[N:52])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[OH-].[Na+].C[Si](C=[N+]=[N-])(C)C>O1CCCC1.CO>[Cl:1][C:2]1[C:3](/[CH:15]=[CH:14]/[C:17]#[N:52])=[C:7]([CH:8]=[CH:9][CH:10]=1)[C:6]([O:5][CH3:4])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 14798Sodium HydroxideHCID 670143-Chlorophthalic anhydrideHCID 85524(Triphenylphosphoranylidene)acetonitrileHCID 167693TrimethylsilyldiazomethaneHCID 16710494Lithium tri-tert-butoxyaluminohydride

생성물 1

HCID 66818998(E)-Methyl 3-chloro-2-(2-cyanovinyl)benzoate

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To 4-chloroisobenzofuran-1,3-dione (1.82 g, 10 mmol) in tetrahydrofuran (20 mL) was added lithium tri-tert-butoxyaluminum hydride (0.5 M, 20 mL, 10 mmol, diglyme) at −20° C. The mixture was stirred at room temperature overnight. (Triphenylphosphoranylidene)acetonitrile (3.0 g, 10 mmol) was added, and the resultant mixture was heated at 120° C. for 16 hours. 2 N Sodium hydroxide(aq) was added and the mixture was extracted with ethyl acetate (2×). HCl(aq) (1 M) was added to the aqueous layer to pH3, and the mixture was extracted with ethyl acetate. The organic extracts was dried and concentrated. The residue was dissolved in 20 mL of 1:1 CH2Cl2:methanol followed by the addition of (trimethylsilyl)diazomethane (4 mL, 2 N in diethyl ether, 8 mmol). The mixture was stirred for 1 hour and quenched with acetic acid. The mixture was concentrated and purified by silica gel column chromatography eluting with 2:1 hexanes:ethyl acetate to afford the title compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.85 (dd, J=1.0, 7.5 Hz, 1H), 7.81 (dd, J=1.0, 8.0 Hz, 1H), 6.04 (d, J=17 Hz, 1H), and 3.84 (s, 3H).

후처리

  1. extractionthe mixture was extracted with ethyl acetate (2×)
  2. additionHCl(aq) (1 M) was added to the aqueous layer to pH3
  3. extractionthe mixture was extracted with ethyl acetate
  4. customThe organic extracts was dried
  5. concentrationconcentrated
  6. dissolutionThe residue was dissolved in 20 mL of 1:1 CH2Cl2
  7. stirringThe mixture was stirred for 1 hour
  8. customquenched with acetic acid
  9. concentrationThe mixture was concentrated
  10. custompurified by silica gel column chromatography
  11. washeluting with 2:1 hexanes

출처 및 근거

ORD 기록
ord-33e43648740e404e89c6ce21cec9b64f
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846951B2

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