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Dimethylformamide → HCID 14370897, 화합물

HRID 2165334
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HRID 2165334 반응식
CN([CH:4]=[O:5])C.[CH2:6]([O:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([OH:28])=[O:27])=[CH:21][CH:20]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].Br[CH:30]([CH3:34])[C:31](O)=[O:32].[C:35](=O)([O-])[O-].[K+].[K+]>O>[CH2:6]([O:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([O:28][CH:30]([C:31]([O:5][CH2:4][CH3:35])=[O:32])[CH3:34])=[O:27])=[CH:21][CH:20]=1)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 117292-Bromopropionic acidHCID 10336152Benzeneacetic acid, 4-(dodecyloxy)-

생성물 1

HCID 14370897HCID 14370897, 화합물수율 76%

시약·촉매·용매 1

HCID 962Water용매

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온도
80 °C

실험 절차

To a DMF solution (30 ml) of 4-dodecyloxyphenylacetic acid (2.4 g, 7.5 mmol.) and 2-bromopropionic acid (1.5 g, 8 mmol.) was added potassium carbonate (1.5 g, 10 mmol.). The mixture was stirred at 80° C. for 2 hours. The reaction solution was cooled, to which was added water (50 ml). The mixture was subjected to extraction with IPE. The organic layer was washed with water, dried and concentrated under reduced pressure. The concentrate was purified by means of a silica gel chromatography (developing solvent: IPE) to give 1-ethoxycarbonylethyl 4-dodecyloxyphenylacetate (2-i, 2.4 g, 76%).

후처리

  1. temperatureThe reaction solution was cooled, to which
  2. extractionThe mixture was subjected to extraction with IPE
  3. washThe organic layer was washed with water
  4. customdried
  5. concentrationconcentrated under reduced pressure
  6. customThe concentrate was purified by means of a silica gel chromatography (developing solvent: IPE)

출처 및 근거

ORD 기록
ord-e91a960c508948bd8dff69722ce7e319
출처 데이터셋
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04939274

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