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Hydrochloric Acid → HCID 19622754, 화합물

HRID 1684032
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인쇄 미리보기

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HRID 1684032 반응식
[CH:1](=[O:13])[C:2]1[CH:12]=[C:9]([O:10][CH3:11])[C:7]([OH:8])=[C:4]([O:5][CH3:6])[CH:3]=1.I[CH2:15][CH2:16][OH:17].C(=O)([O-])[O-].[K+].[K+].Cl>O.CN(C=O)C>[CH3:11][O:10][C:9]1[CH:12]=[C:2]([CH:3]=[C:4]([O:5][CH3:6])[C:7]=1[O:8][CH2:15][CH2:16][OH:17])[CH:1]=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 8655SyringaldehydeHCID 11430Potassium CarbonateHCID 12225Iodoethanol

생성물 1

HCID 19622754HCID 19622754, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 6228
Dimethylformamide
용매

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온도
80 °C

실험 절차

Syringaldehyde (1.0 g, 5.49 mmole), 2-iodo-1-ethanol (1.90 g, 10.98 mmole) and potassium carbonate (1.90 g, 13.77 mmole) are added to 15 ml dry DMF and stirred for 24 hours at 80° C. under an argon atmosphere. The reaction mixture is added to 100 ml H2O and acidified with 10% HCl. The product is extracted into CHCl3, dried over MgSO4, and concentrated to an oil in vacuo. The remaining oil is purified by flash column chromatography using 1:1 hex/ethyl acetate as eluent (1.009 g, 81%).

후처리

  1. extractionThe product is extracted into CHCl3
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated to an oil in vacuo
  4. customThe remaining oil is purified by flash column chromatography

출처 및 근거

ORD 기록
ord-b9bfcc5ff90e47df8b3dbd8987a9c061
출처 데이터셋
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05639782

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