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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Bicarbonate → HCID 20430688, 화합물

HRID 2413207
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HRID 2413207 반응식
[C:1]1([C:6]2([CH2:11][OH:12])[CH2:10][CH:9]=[CH:8]O2)[CH2:5][CH2:4][CH2:3][CH:2]=1.C(=O)([O-])[OH:14].[Na+]>CC(C)=O.O>[OH:14][CH:10]1[CH:9]=[CH:8][C:11](=[O:12])[CH:6]1[CH:1]1[CH2:5][CH2:4][CH:3]=[CH:2]1
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참가 물질

5

반응물 2

HCID 516892Sodium BicarbonateHCID 70488488HCID 70488488, 화합물

생성물 1

HCID 20430688HCID 20430688, 화합물수율 55%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

실험 절차

2-Cyclopentenyl-2-furyl methanol (131 g, 0.8 mole) was dissolved in a 2:1 mixture (1.5 liters) of acetone and water in a reactor, and polyphosphoric acid (20 g) was added thereto. Thereafter, reaction was carried out at 50° to 60° C. for about 24 hours with stirring. After completion of the reaction, the reaction solution was cooled and neutralized with addition of a saturated aqueous solution (200 ml) of sodium hydrogen carbonate, followed by extraction with a solvent. The extract was washed with water, dried and concentrated. The residue obtained was distilled under reduced pressure to obtain 72 g (yield, 55%) of pure (±)-3-hydroxy-2-(2-cyclopentenyl)-4-cyclopenten-1-one having a boiling point of 115°-120° C./3 mmHg.

후처리

  1. customThereafter, reaction
  2. customAfter completion of the reaction
  3. temperaturethe reaction solution was cooled
  4. extractionfollowed by extraction with a solvent
  5. washThe extract was washed with water
  6. customdried
  7. concentrationconcentrated
  8. customThe residue obtained
  9. distillationwas distilled under reduced pressure

출처 및 근거

ORD 기록
ord-e7a41dd057f74426b25bf6726f847bfe
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04496586

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