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Tetrahydrofuran → (2-Methoxy-4-propylphenyl)methanol

HRID 602832
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HRID 602832 반응식
COCCO[AlH2-]O[CH2:8][CH2:9][O:10][CH3:11].[Na+].[C:13]1(C)[CH:18]=CC=[CH:15][CH:14]=1.[O:20]1[CH2:24][CH2:23][CH2:22][CH2:21]1.O.O.O.O.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>CO>[CH3:11][O:10][C:9]1[CH:8]=[C:18]([CH2:13][CH2:14][CH3:15])[CH:24]=[CH:23][C:22]=1[CH2:21][OH:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 2724148Sodium potassium tartrate tetrahydrateHCID 131728749Red-Al toluene

생성물 1

HCID 59582157(2-Methoxy-4-propylphenyl)methanol

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
35 °C

실험 절차

Red-Al/toluene solution (66.5% content, 2.05 g) was slowly added to a tetrahydrofuran (3 mL) solution of the compound (1.00 g) prepared in Example 43 at an internal temperature of 5° C., followed by stirring at an internal temperature of about 35° C. for about 2.5 hours. Methanol (0.5 mL) was added to the reaction solution at an internal temperature of 9° C. to stop the reaction. The reaction solution was poured into a 50% aqueous potassium sodium tartrate tetrahydrate solution, and extracted with ethyl acetate. The organic layer was successively washed with water and brine, dried, and concentrated, to thereby obtain the title compound (0.91 g) having the following physical properties.

후처리

  1. customthe reaction
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was successively washed with water and brine
  4. customdried
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9ec1c87a7cba46e6aae4812c5107099d
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07906549B2

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