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Hydrochloric Acid → 2-Benzylacrylic Acid

HRID 1005302
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HRID 1005302 반응식
[CH2:1]([CH:8]([C:12](O)=O)[C:9]([OH:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(NCC)C.C=O.Cl>O>[CH2:1]([C:8](=[CH2:12])[C:9]([OH:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 712FormaldehydeHCID 8021DiethylamineHCID 12031Benzylmalonic acid

생성물 1

HCID 3035712-Benzylacrylic Acid수율 78%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a cooled (0° C.) mixture of benzyl malonic acid (3.37 g, 17.4 mmol) and diethylamine (1.34 g, 18.3 mmol) in water (10 ml) was added formaldehyde (37% solution in water, 2.1 g, 26.1 mmol) with stirring. The reaction was allowed to warm to room temperature and after 2 hours heated to reflux. After 16 hours, the reaction mixture was cooled to room temperature, then made acidic with hydrochloric acid. The mixture was extracted twice with ethyl acetate. The ethyl acetate layers were combined and dried over sodium sulfate, then the solvent was removed under reduced pressure. The resulting residue was purified by column chromatography to yield 2.2 g (78%) of white solid. 1H NMR (CDCl3): δ 3.7 (s, 2H), 5.6 (s, 1H) , 6.4 (s, 1H) , 7.1-7.4 (m, 5H)

후처리

  1. temperatureTo a cooled
  2. temperatureheated to reflux
  3. temperaturethe reaction mixture was cooled to room temperature
  4. extractionThe mixture was extracted twice with ethyl acetate
  5. dry with materialdried over sodium sulfate
  6. customthe solvent was removed under reduced pressure
  7. customThe resulting residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-ff9c21a164d4487c82f295ce909f0292
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06054444

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