p-Toluenesulfonic acid → Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate

HRID 2364731노트

반응식

HRID 2364731 반응식
[CH2:1]([C:4]1[C:13]([OH:14])=[C:12]([N+:15]([O-:17])=[O:16])[CH:11]=[CH:10][C:5]=1[C:6]([O:8][CH3:9])=[O:7])[CH:2]=[CH2:3].C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+]>ClCCCl>[CH3:3][CH:2]1[CH2:1][C:4]2=[C:5]([C:6]([O:8][CH3:9])=[O:7])[CH:10]=[CH:11][C:12]([N+:15]([O-:17])=[O:16])=[C:13]2[O:14]1

참가 물질

5

반응물 3

HCID 6101p-Toluenesulfonic acidHCID 516892Sodium BicarbonateHCID 59768300Methyl 2-allyl-3-hydroxy-4-nitro-benzoate

생성물 1

HCID 68107419Methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate수율 12.8%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

Methyl 2-allyl-3-hydroxy-4-nitro-benzoate 1d (800 mg, 3.30 mmol) was dissolved in 10 mL of 1,2-dichloroethane followed by the addition of 1 mL of p-toluenesulfonic acid. The reaction solution was stirred for 48 hours. The resulting solution was added with 10 mL of saturated sodium bicarbonate solution and extracted with dichloromethane (20 mL×3). The combined organic phase was washed with water (20 mL) and saturated sodium chloride solution (20 mL) successively, then dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound methyl 2-methyl-7-nitro-2,3-dihydrobenzofuran-4-carboxylate 30a (100 mg, yield: 12.5%) as a yellow solid.

후처리

  1. extractionextracted with dichloromethane (20 mL×3)
  2. washThe combined organic phase was washed with water (20 mL) and saturated sodium chloride solution (20 mL) successively
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe resulting residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-51351d0447ac4bdabd5a60488bdc8bee
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08691822B2

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