Hydrochloric Acid → 4'-(Hydroxymethyl)-[1,1'-Biphenyl]-2-Carboxylic Acid

HRID 743757노트

반응식

HRID 743757 반응식
CC1(C)C[O:5][C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[C:13]2[CH:18]=[CH:17][C:16]([CH2:19][OH:20])=[CH:15][CH:14]=2)=N1.Cl.C([OH:25])C>>[OH:20][CH2:19][C:16]1[CH:17]=[CH:18][C:13]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[C:4]([OH:5])=[O:25])=[CH:14][CH:15]=1

참가 물질

4

반응물 3

HCID 313Hydrochloric Acid2회HCID 702EthanolHCID 110658764,4-Dimethyl-2-(4'hydroxymethylbiphenyl-2-yl)oxazoline

생성물 1

HCID 153808804'-(Hydroxymethyl)-[1,1'-Biphenyl]-2-Carboxylic Acid수율 81%

실험 절차

2.0 g (7.11 mmol) of 4,4-dimethyl-2-(4'-hydroxymethylbiphenyl-2-yl)oxazoline was dissolved in ethanol (30 ml). 2N hydrochloric acid (10 ml) was added thereto, followed by heating under reflux for 3 hours. After the reaction liquid was cooled and concentrated, a saturated aqueous solution of sodium hydrogen-carbonate (100 ml) was added thereto, followed by the extraction with chloroform. After the organic phase was washed with water and dried, it was subjected to vacuum concentration. A 20% aqueous solution of sodium hydroxide (20 ml) and ethanol (20 ml) were added to the residue, followed by heating under reflux for 8 hours. After the reaction liquid was cooled to room temperature and adjusted to pH 6 with hydrochloric acid, it was extracted with chloroform. After the organic phase was washed with water and dried, it was subjected to vacuum concentration. The residue was purified by silica gel column chromatography (a chloroform/methanol system) to give 1.31 g of the title compound (yield 81%).

후처리

  1. temperatureby heating
  2. temperatureunder reflux for 3 hours
  3. customAfter the reaction liquid
  4. temperaturewas cooled
  5. concentrationconcentrated
  6. additiona saturated aqueous solution of sodium hydrogen-carbonate (100 ml) was added
  7. extractionfollowed by the extraction with chloroform
  8. washAfter the organic phase was washed with water
  9. customdried
  10. concentrationit was subjected to vacuum concentration
  11. additionA 20% aqueous solution of sodium hydroxide (20 ml) and ethanol (20 ml) were added to the residue
  12. temperatureby heating
  13. temperatureunder reflux for 8 hours
  14. customAfter the reaction liquid
  15. extractionwas extracted with chloroform
  16. washAfter the organic phase was washed with water
  17. customdried
  18. concentrationit was subjected to vacuum concentration
  19. customThe residue was purified by silica gel column chromatography (a chloroform/methanol system)

출처 및 근거

ORD 기록
ord-af8c0ff7ce60438881776cc7f2b8b4d7
출처 데이터셋
uspto-grants-1996_09
특허 번호
US05557002

반응 노트

불러오는 중…