(3,5-Dimethoxyphenyl)acetic acid → 2-(3,5-Dimethoxyphenyl)ethanol

HRID 253740

반응식

HRID 253740 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH3:7][O:8][C:9]1[CH:10]=[C:11]([CH2:17][C:18](O)=[O:19])[CH:12]=[C:13]([O:15][CH3:16])[CH:14]=1>O1CCOCC1>[CH3:16][O:15][C:13]1[CH:12]=[C:11]([CH:10]=[C:9]([O:8][CH3:7])[CH:14]=1)[CH2:17][CH2:18][OH:19]

참가 물질

4

반응물 2

HCID 138316(3,5-Dimethoxyphenyl)acetic acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 2656342-(3,5-Dimethoxyphenyl)ethanol수율 103.2%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

반응 조건

온도
50 °C

실험 절차

To a mixture of LiAlH4 (1.05 g) in dioxane (100 ml) was added a solution of 3,5-dimethoxyphenyl acetic acid (5.32 g) in dioxane (20 ml) portionwise at 0° C. The mixture was stirred at room temperature for 0.5 hour and at 50° C. for 2 hours. The mixture was quenched with conc. NH4OH and filtered through Celite. The filtrate was evaporated to yield 3,5-dimethoxyphenethyl alcohol (5.1 g). IR (Neat) 3400, 1600 cm−1; MS (GC−EI) 182 (M+), 151 (M−MeO).

후처리

  1. customThe mixture was quenched with conc. NH4OH
  2. filtrationfiltered through Celite
  3. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-a9098927c3794d0688533a49c4db6ecf
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07872151B2

연결된 노트

불러오는 중…