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Tetrahydrofuran → Phthalide

HRID 1763860
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HRID 1763860 반응식
Cl[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[O:3]1.O1CCCC1>[Ni].C(N(CC)CC)C>[C:4]1([C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[CH2:2][O:3]1)=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8028TetrahydrofuranHCID 954693-Chlorophthalide

생성물 1

HCID 6885Phthalide수율 89%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 8471Triethylamine용매

반응 조건

온도
65 °C

실험 절차

A 1-liter lift magnet autoclave is charged with 110 g of 3-chlorophthalide, 10 g of nickel catalyst RCH 55/10 (commercial product of Farbwerke Hoechst AG) and 400 ml of tetrahydrofuran to which 66 g of triethylamine is added. After purging the air with nitrogen, hydrogen is pumped in to a pressure of 10 bars, and the temperature is raised, with stirring, to 65° C. The hydrogen consumption is compensated by additions in the range between 10 and 20 bars for a period of 41/2 hours. After the absorption of hydrogen ceases, the catalyst and precipitated salt are filtered out and the solvent is withdrawn. After distillation of the residue between 88° and 90° C. and 0.2 Torr, 77.5 g of phthalide is obtained, of a melting point of 71° C. (gas-chromatographic analysis 98.95%).

후처리

  1. additionis added
  2. customAfter purging the air with nitrogen, hydrogen
  3. temperaturethe temperature is raised
  4. customThe hydrogen consumption
  5. customAfter the absorption of hydrogen ceases
  6. customthe catalyst and precipitated salt
  7. filtrationare filtered out
  8. customthe solvent is withdrawn
  9. distillationAfter distillation of the residue between 88° and 90° C. and 0.2 Torr

출처 및 근거

ORD 기록
ord-90dc5f675c134927943a8a045da7c888
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04113741

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