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HCID 69365855, 화합물 → 4-(2-Phenylethyl)oxolan-2-one

HRID 8196
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HRID 8196 반응식
CO[C:3](=[O:23])[CH:4]=[C:5]([CH2:14][O:15]CC1C=CC=CC=1)[CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>[Pd].C(O)(=O)C>[CH2:6]([CH:5]1[CH2:14][O:15][C:3](=[O:23])[CH2:4]1)[CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 69365855HCID 69365855, 화합물

생성물 1

HCID 137049024-(2-Phenylethyl)oxolan-2-one수율 62%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 176Acetic Acid용매

실험 절차

A mixture of 3-benzyloxymethyl-5-phenyl-pent-2-enoic acid methyl ester, (3.2 g, 13.5 mmol), 10 wt. % palladium on activated carbon (3.2 g), and acetic acid (40 mL) is placed in a Parr® Shaker under hydrogen (45 PSI) and shaken 4 h. The mixture is filtered through a pad of Celite® and concentrated in vacuo. The residue is dissolved in toluene (30 mL), treated with p-tolunesulfonic acid (0.1 g), refluxed for 2 h and concentrated in vacuo. The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes then 50% ethyl acetate/hexanes) to yield the title compound 1.2 g (62%) as a colorless liquid.

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후처리

  1. filtrationThe mixture is filtered through a pad of Celite®
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue is dissolved in toluene (30 mL)
  4. additiontreated with p-tolunesulfonic acid (0.1 g)
  5. temperaturerefluxed for 2 h
  6. concentrationconcentrated in vacuo
  7. customThe residue is chromatographed on SiO2 (10% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-d114d255e7104c6da67a11cdcb488991
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07087626B2

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