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

HRID 1474276노트

반응식

HRID 1474276 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 stir 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 column 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. stirringto stir 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 column chromatography

출처 및 근거

ORD 기록
ord-71d284e30b2d44d891637f685b3187c8
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09018211B2

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