Ethyl diethoxyacetate → methyl 5-bromo-3,4-dihydro-1H-isochromene-1-carboxylate

HRID 1187018노트

반응식

HRID 1187018 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][OH:10].[CH2:11]([O:13][CH:14]([O:20]CC)[C:15](OCC)=O)C>C[N+]([O-])=O.Cl[Ti](Cl)(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[CH2:8][CH2:9][O:10][CH:15]2[C:14]([O:13][CH3:11])=[O:20]

참가 물질

5

반응물 2

HCID 80169Ethyl diethoxyacetateHCID 27340892-(2-Bromophenyl)ethan-1-ol

생성물 1

HCID 66646338methyl 5-bromo-3,4-dihydro-1H-isochromene-1-carboxylate

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 6375Nitromethane용매

실험 절차

TiCl4 (76 g, 0.4 mol) was added over a period of 10 min to an ice-cooled mixture of 2-(2-bromophenyl)ethanol (20 g, 0.1 mol) and ethyl bis(ethyloxy)acetate (21.1 g, 0.120 mol) in 120 mL of CH3NO2. After stirring for 10 min, the ice bath was removed and the mixture was allowed to stire at room temperature overnight. The mixture was poured into ice/aqueous 1N HCl. Extracted with DCM and backwashed with 1N HCl and brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified with silica gel cloumn chromatography to give the product methyl 5-bromo-3,4-dihydro-1H-isochromene-1-carboxylate.

후처리

  1. temperaturecooled
  2. customthe ice bath was removed
  3. waitto stire at room temperature overnight
  4. additionThe mixture was poured into ice/aqueous 1N HCl
  5. extractionExtracted with DCM
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customThe residue was purified with silica gel cloumn chromatography

출처 및 근거

ORD 기록
ord-8bb0d34d662840e5ae2a85da065b52be
출처 데이터셋
uspto-grants-2014_03
특허 번호
US08673920B2

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