Hydrochloric Acid → 5-Cyano-2-[2-(4-methoxyphenyl)ethyl]-3-benzofurancarboxylic acid

HRID 53968노트

반응식

HRID 53968 반응식
[OH-:1].[Na+].BrBr.[C:5]([C:8]1[C:12]2[CH:13]=[C:14]([C:17]#[N:18])[CH:15]=[CH:16][C:11]=2[O:10][C:9]=1[CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=1)(=[O:7])C.Cl>O.O1CCOCC1>[C:17]([C:14]1[CH:15]=[CH:16][C:11]2[O:10][C:9]([CH2:19][CH2:20][C:21]3[CH:22]=[CH:23][C:24]([O:27][CH3:28])=[CH:25][CH:26]=3)=[C:8]([C:5]([OH:1])=[O:7])[C:12]=2[CH:13]=1)#[N:18]

참가 물질

7

실험 절차

5.2 g of sodiumhydroxide was dissolved in 30 ml of water, and the solution was cooled to a temperature of 0° C. or below. With stirring, to this were added dropwise 2.7 ml of bromine and then 40 ml of a dioxane solution containing 4.14 g of 3-acetyl-2-[2-(4-methoxyphenyl)ethyl]-5-benzofurancarbonitrile obtained in the above step d). The resulting mixture was stirred at 0° C. for 45 minutes with ice cooling for 1 hour. The resulting reaction solution was mixed with water, adjusted to pH 2 with concentrated hydrochloric acid, and then extracted with chloroform. The resulting organic layer was washed with water and dried to distill off the solvent. Thereafter, the resulting residue was purified by subjecting it to silica gel column chromatography using chloroform as an eluant, thereby obtaining 1.44 g of 5-cyano-2-[2-(4-methoxyphenyl)ethyl]-3-benzofurancarboxylic acid.

후처리

  1. temperaturethe solution was cooled to a temperature of 0° C. or below
  2. customobtained in the above step d)
  3. stirringThe resulting mixture was stirred at 0° C. for 45 minutes with ice cooling for 1 hour
  4. customThe resulting reaction solution
  5. extractionextracted with chloroform
  6. washThe resulting organic layer was washed with water
  7. customdried
  8. distillationto distill off the solvent
  9. customThereafter, the resulting residue was purified

출처 및 근거

ORD 기록
ord-760acea9f09f4125a5e816086c5487cb
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05620991

반응 노트

불러오는 중…