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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 72483452, 화합물 → HCID 68448656, 화합물

HRID 2220575
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HRID 2220575 반응식
[CH2:1]([O:3][C:4]1[CH:21]=[CH:20][C:7]2[CH:8]3[CH2:14][CH2:13][CH:12]([CH:15]=[CH:16][CH2:17][CH2:18][CH3:19])[CH2:11][CH:9]3[O:10][C:6]=2[C:5]=1[F:22])[CH3:2].[H][H]>C1COCC1.[Pd]>[CH2:1]([O:3][C:4]1[CH:21]=[CH:20][C:7]2[CH:8]3[CH2:14][CH2:13][CH:12]([CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])[CH2:11][CH:9]3[O:10][C:6]=2[C:5]=1[F:22])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 72483452HCID 72483452, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 68448656HCID 68448656, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

5.1 g (about 10.7 mmol) of (E/Z) isomer mixture of (±)-(3R*, 4aR*, 9bS*)-7-ethoxy-6-fluoro-3-pent-1-enyl-1,2,3,4,4a,9b-hexahydrodibenzofuran in 50 ml of THF are hydrogenated in a hydrogen atmosphere with addition of 5.0 g of Pd/C (5% Pd). After completion of the uptake of hydrogen (37 h), the reaction solution is filtered and concentrated to dryness. The residue is filtered adsorptively (SiO2, toluene), and the beige solid obtained is re-crystallised repeatedly from isopropanol at room temperature, giving (±)-(3R*, 4aR*, 9bS*)-7-ethoxy-6-fluoro-3-pentyl-1,2,3,4,4a,9b-hexahydro-dibenzofuran as colourless solid (melting point 118° C.).

후처리

  1. filtrationAfter completion of the uptake of hydrogen (37 h), the reaction solution is filtered
  2. concentrationconcentrated to dryness
  3. filtrationThe residue is filtered adsorptively (SiO2, toluene)
  4. customthe beige solid obtained
  5. customis re-crystallised repeatedly from isopropanol at room temperature

출처 및 근거

ORD 기록
ord-829fea35312b4cae98992136e3e4c195
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07417157B2

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