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Methanol → HCID 20059823, 화합물

HRID 232384
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인쇄 미리보기

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HRID 232384 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([CH3:15])[C:12]([CH2:16][C:17]([O:19]CC2C=CC=CC=2)=[O:18])=[C:11]([CH3:27])[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CO.[OH-].[Na+]>O>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH3:27])[C:12]([CH2:16][C:17]([OH:19])=[O:18])=[C:13]([CH3:15])[CH:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 20059716HCID 20059716, 화합물

생성물 1

HCID 20059823HCID 20059823, 화합물수율 80%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

0.35 g of benzyl 2-(4-benzyloxy-2,6-dimethylphenyl)acetate was shaken overnight with a mixture of 7 ml of methanol, 0.7 ml of water and 0.28 g of solid sodium hydroxide. The resulting solution was evaporated and the residue was partitioned between 50 ml of methylene chloride and 25 ml of 2M hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate and evaporated. The solid residue was recrystallized from a mixture of 3 ml of methanol and 3 ml of water to give 0.21 g of 2-(4-benzyloxy-2,6-dimethylphenyl)acetic acid of melting point 149°-150° C.

후처리

  1. customThe resulting solution was evaporated
  2. customthe residue was partitioned between 50 ml of methylene chloride and 25 ml of 2M hydrochloric acid
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. customevaporated
  5. customThe solid residue was recrystallized from a mixture of 3 ml of methanol and 3 ml of water

출처 및 근거

ORD 기록
ord-d835f946c7644b60a06fd60219d6c004
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04851519

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