Benzyl Chloride → 2,5-bis(benzyloxy)benzoic acid

HRID 614819

반응식

HRID 614819 반응식
[CH2:1]([O:8][C:9]1[CH:18]=[C:13]([C:14]([O:16]C)=[O:15])[C:12]([OH:19])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:26](Cl)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.[OH-].[Na+]>S1(CCCC1)(=O)=O.O>[CH2:26]([O:19][C:12]1[CH:11]=[CH:10][C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:18][C:13]=1[C:14]([OH:16])=[O:15])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

참가 물질

7

실험 절차

A mixture of methyl gentisate (16.8 g) and anhydrous potassium carbonate (7.0 g) in dry sulpholane (150 ml) was treated, with stirring, with benzyl chloride (12.7 g), and the mixture was stirred and heated at 100° C. for 4 hours. The mixture was then poured into water (800 ml) and the separated solid was filtered off and recrystallized from ethanol (with the aid of charcoal) to give methyl 5-benzyloxysalicylate (10.7 g), m.p. 108°-112° C. This ester (9.2 g) was heated at 150° C. for 3 hours with a mixture of anhydrous potassium carbonate (2.5 g) and benzyl chloride (4.52 g) in dry sulpholane (100 ml) and the mixture was then cooled and poured into a mixture of ice and water (700 ml), and the mixture was extracted with diethyl ether (2 × 300 ml). The ether extracts were combined and evaporated, the residual oil was triturated with water (100 ml), the oil was separated and the aqueous layer was extracted with diethyl ether (25 ml). The combined oil and extracts were washed with brine, dried over magnesium sulphate and evaporated to give crude methyl 2,5-dibenzyloxybenzoate (12.7 g). This ester (12.4 g) was heated at reflux with aqueous sodium hydroxide solution (2N; 400 ml) for 2 hours and allowed to cool. The separated sodium salt was filtered off and ground with hydrochloric acid (6N; 100 ml), the mixture was heated at reflux for 5 minutes and then cooled. The solid which separated was filtered off, washed with water and dried to give 2,5-dibenzyloxybenzoic acid (8.2 g), m.p. 107°-108.5° C.

후처리

  1. temperaturethe mixture was then cooled
  2. extractionthe mixture was extracted with diethyl ether (2 × 300 ml)
  3. customevaporated
  4. customthe residual oil was triturated with water (100 ml)
  5. customthe oil was separated
  6. extractionthe aqueous layer was extracted with diethyl ether (25 ml)
  7. washThe combined oil and extracts were washed with brine
  8. dry with materialdried over magnesium sulphate
  9. customevaporated
  10. customto give crude methyl 2,5-dibenzyloxybenzoate (12.7 g)
  11. temperatureto cool
  12. filtrationThe separated sodium salt was filtered off
  13. temperatureground with hydrochloric acid (6N; 100 ml), the mixture was heated
  14. temperatureat reflux for 5 minutes
  15. temperaturecooled
  16. customThe solid which separated
  17. filtrationwas filtered off
  18. washwashed with water
  19. customdried

출처 및 근거

ORD 기록
ord-d067d0c1be8744f3aa30a4a8b75222bc
출처 데이터셋
uspto-grants-1979_03
특허 번호
US04146631

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