Hydrochloric Acid → 4-(4-Hydroxybutoxy)phenol

HRID 36154

반응식

HRID 36154 반응식
[OH:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][CH2:7][CH2:8][CH2:9][C:10](OCC)=[O:11])=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.Cl>CCOCC>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][OH:11])=[CH:15][CH:16]=1

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 189185904-(4-Hydroxy-phenoxy)-butyric acid ethyl esterHCID 21226445Aluminium lithium hydride

생성물 1

HCID 224080554-(4-Hydroxybutoxy)phenol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 5.07 g of ethyl 4-(4-hydroxyphenoxy)butyrate in 23 ml of ether is added dropwise to a mixture of 1.72 g of lithium aluminum hydride in 90 ml of ether at a rate which maintains a gentle reflux. The mixture is stirred at ambient temperature for 6 hours, and then water is carefully added followed by 3N HCl to dissolve all solids. After separating the ether phase and extracting the aqueous phase twice with ether, the combined ether phases are washed with saturated NaHCO3, water, and brine and dried over MgSO4. Filtration and concentration yields 4-(4-hydroxyphenoxy)butan-1-ol as a white solid.

후처리

  1. dissolutionto dissolve all solids
  2. customAfter separating the ether phase
  3. extractionextracting the aqueous phase twice with ether
  4. washthe combined ether phases are washed with saturated NaHCO3, water, and brine
  5. dry with materialdried over MgSO4
  6. filtrationFiltration and concentration

출처 및 근거

ORD 기록
ord-1a2fddbefda64ab5ad9c76a4ab7e530b
출처 데이터셋
uspto-grants-1995_05
특허 번호
US05412137

연결된 노트

불러오는 중…