3,4-Dihydroxybenzaldehyde → 3-Benzyloxy-4-hydroxybenzaldehyde

HRID 2186521노트

반응식

HRID 2186521 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[OH:10])[CH:5]=[O:6].[OH-].[K+]>>[CH2:5]([O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[OH:10])[CH:5]=[O:6])[C:4]1[CH:7]=[CH:8][CH:9]=[CH:2][CH:3]=1

참가 물질

3

반응물 2

HCID 87683,4-DihydroxybenzaldehydeHCID 14797Potassium Hydroxide

생성물 1

HCID 110206353-Benzyloxy-4-hydroxybenzaldehyde수율 59.8%

실험 절차

To a mixture of 3,4-dihydroxy benzaldehyde (40.80 gms, 0.29 mol) and ethanolic potassium hydroxide (2 N, 320 mL) benzylchloride (37.54 g, 0.29 mol) was added slowly at room temperature. The reaction mixture was stirred overnight under nitrogen. The ethanol was removed on rotavapour and remaining solution treated with ice water. For removal of dibenzyl ether alkaline solution was extracted with diethyl ether (500 ml). Then the aqueous layer was acidified with concentrated hydrochloric acid and extracted thrice with ethyl acetate (800 ml). The organic layer was dried (Na2SO4), filtered and concentrated. The crude product was purified on silica gel column using EtOAc:light petroleum (1:9) as eluent to give 3-bezyloxy-4-hydroxy benzaldehyde (19.80 g, 29%). TLC: Ethyl acetate:light petroleum (1:4), Rf=0.3; m.p: 109-111° C.; 1H NMR (CDCl3, 200 MHz): δ 5.06 (s, 2H), 6.39 (s,1H), 6.95 (d, J=8.0 Hz, 1H), 7.1-7.4 (m, 7H) and 9.57 (s, 1H).

후처리

  1. additionwas added slowly at room temperature
  2. customThe ethanol was removed on rotavapour
  3. additiontreated with ice water
  4. customFor removal of dibenzyl ether alkaline solution
  5. extractionwas extracted with diethyl ether (500 ml)
  6. extractionextracted thrice with ethyl acetate (800 ml)
  7. dry with materialThe organic layer was dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude product was purified on silica gel column

출처 및 근거

ORD 기록
ord-8cafce57775948378e9ad338c04e4914
출처 데이터셋
uspto-grants-2002_06
특허 번호
US06403814B1

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